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Sector Probe S4-2 A7CA

by Konica Minolta, Inc.

Ref S4-2Model SECTOR PROBE S4-2

Sector Probe S4-2 A7CA is a device classified as Class IIa in the EU and Class II in the US made by Konica Minolta, Inc., registered in EUDAMED on 2 Jul 2026 (Basic UDI-DI 4560141920000598S), cleared under FDA 510(k) K151060 on 5 Jun 2015 and listed in FDA GUDID since 19 Sep 2016 (UDI-DI 04560141940185), active as of 24 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None ongoing

1 closed

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K151060

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4560141920000598S Basic UDI-DI 04560141940185UDI-DIDate2 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04560141940185 UDI-DI Date19 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK151060 Date5 Jun 2015DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 4560141920000598S registered 2 Jul 2026 Active
  • FDA 510(k) K151060 decided 5 Jun 2015 Active
  • FDA GUDID UDI-DI 04560141940185 listed 19 Sep 2016 Listed

Recalls

1 recall · FDA

    • Terminated Z-1215-2018 FDA Class II initiated 4 Dec 2017 on shared 510(k) K151060

    There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Timeline

4 dated events

  1. Cleared FDA 510(k) K151060
  2. Listed FDA GUDID 04560141940185
  3. Recall initiated FDA recalls Z-1215-2018
  4. Registered EUDAMED 4560141920000598S

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Sector Probe S4-2
Generic name
Extracorporeal ultrasound imaging transducer, hand-held
Model / reference
SECTOR PROBE S4-2 EUDAMED
S4-2 EUDAMED
A7CA GUDID
Primary DI / UDI-DI
04560141940185
Basic UDI-DI
4560141920000598S
Direct marketing DI
04560141940185
510(k) Number
FDA product code
ITX
EMDN code
Z110402010301 Transcutaneous ultrasound sector probes (phased array), two–dimensional
GMDN term
Extracorporeal ultrasound imaging transducer, hand-held
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
892.1570
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
SECTOR PROBE S4-2
S4-2
GUDID
A7CA
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Extracorporeal ultrasound imaging transducer, hand-held

Cleared under the same submission (K151060)

Similar devices in this category

Other devices filed under TRANSCUTANEOUS ULTRASOUND SECTOR PROBES (PHASED ARRAY), TWO–DIMENSIONAL.

Other devices from Konica Minolta, Inc.

See all devices from Konica Minolta, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (23, all answered No)