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Sonic Window Docking Station

FDA UDI

Class II (US FDA UDI)

by Analogic Corporation

Identity

Trade Name
Sonic Window Docking Station FDA UDI
Generic Name
Hand-held ultrasound imaging system, body-surface FDA UDI
Device Name
Docking Station for Sonic Window Handheld Ultrasound System FDA UDI
Model / Reference
10-73869-01 FDA UDI
Description
Docking Station for Sonic Window Handheld Ultrasound System FDA UDI

Identifiers

Primary DI / UDI-DI
90814277020011 FDA UDI
510(k) Number
K140126 FDA UDI
FDA Product Code
IYO FDA UDI
IYN FDA UDI
ITX FDA UDI
GMDN Term
Hand-held ultrasound imaging system, body-surface FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.1550 FDA UDI
892.1570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand-held ultrasound imaging system, body-surface

Sonic Window Docking Station by Analogic Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held ultrasound imaging system, body-surface.

Cleared under the same submission

K140126 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Analogic Corporation

Sources (1)

  • FDA UDI 1a01c7a8-2345-427a-8c8a-dbb7f87d1f1c 35 fields · synced Jun 8, 2026