P-71 A9YD

by Konica Minolta, Inc.

P-71 A9YD is a Class II device made by Konica Minolta, Inc., cleared under FDA 510(k) K172793 on 12 Oct 2017 and listed in FDA GUDID since 25 Jan 2018 (UDI-DI 04560141945838), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04560141945838 UDI-DI	Date25 Jan 2018Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Special	NumberK172793	Date12 Oct 2017Decided	StatusActive

Official records

AccessGUDID record UDI-DI 04560141945838
FDA 510(k) database 510(k) number K172793

Across registries

2 registries list this device

FDA 510(k) K172793 decided 12 Oct 2017 Active
FDA GUDID UDI-DI 04560141945838 listed 25 Jan 2018 Listed

Timeline

2 dated events

12 Oct 2017 Cleared FDA 510(k) K172793
25 Jan 2018 Listed FDA GUDID 04560141945838

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: P-71
Generic name: Indirect flat panel x-ray detector
Model / reference: A9YD

Primary DI / UDI-DI: 04560141945838
510(k) Number: K172793
FDA product code: MQB
GMDN term: Indirect flat panel x-ray detector

Device class: Class II
Regulation number: 892.1680
GUDID distribution status: In Commercial Distribution

MRI safety: MR Unsafe

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Properties

Prescription use
Serial number

Other properties (13, all answered No)