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Applicator 9201

FDA UDI

Class II (US FDA UDI)

by Mettler Electronics Corp.

Identity

Trade Name
Applicator 9201 FDA UDI
Generic Name
Physical therapy ultrasound system applicator, hand-held FDA UDI
Device Name
920 applicator (Large size/ 1 & 3 MHz) FDA UDI
Model / Reference
9201 FDA UDI
Description
920 applicator (Large size/ 1 & 3 MHz) FDA UDI

Identifiers

Catalog Number
9201 FDA UDI
Primary DI / UDI-DI
00816864020647 FDA UDI
510(k) Number
K111482 FDA UDI
FDA Product Code
IMG FDA UDI
IPF FDA UDI
GZI FDA UDI
GZJ 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
890.5850 FDA UDI
882.5810 FDA UDI
882.5890 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

Applicator 9201 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

K111482 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 b0fc6a32-8299-4b31-a4c6-5a0752849897 37 fields · synced Jun 8, 2026