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Ultrasound Applicator 7431

FDA UDI

Class II (US FDA UDI)

by Mettler Electronics Corp.

Identity

Trade Name
Ultrasound Applicator 7431 FDA UDI
Generic Name
Physical therapy ultrasound system applicator, hand-held FDA UDI
Device Name
740 ultrasound applicator; 1 cm sq., 3 MHz FDA UDI
Model / Reference
7431 FDA UDI
Description
740 ultrasound applicator; 1 cm sq., 3 MHz FDA UDI

Identifiers

Catalog Number
7431 FDA UDI
Primary DI / UDI-DI
00816864020623 FDA UDI
510(k) Number
K053546 FDA UDI
FDA Product Code
IMG FDA UDI
GMDN Term
Physical therapy ultrasound system applicator, hand-held FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5860 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Physical therapy ultrasound system applicator, hand-held

Ultrasound Applicator 7431 by Mettler Electronics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy ultrasound system applicator, hand-held.

Cleared under the same submission

K053546 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mettler Electronics Corp.

Sources (1)

  • FDA UDI a9a2f62e-43fd-4788-8a42-414520718345 37 fields · synced May 30, 2026