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Auto*Therm 390

FDA UDI

Class II (US FDA UDI)

by Mettler Electronics Corp.

Identity

Trade Name
Auto*Therm 390 FDA UDI
Generic Name
Short-wave diathermy treatment system, professional FDA UDI
Device Name
Continuous and pulsed shortwave diathermy with capacitive applicators FDA UDI
Model / Reference
ME 390 FDA UDI
Description
Continuous and pulsed shortwave diathermy with capacitive applicators FDA UDI

Identifiers

Catalog Number
ME 390 FDA UDI
Primary DI / UDI-DI
00816864020180 FDA UDI
510(k) Number
K042554 FDA UDI
FDA Product Code
IMJ FDA UDI
GMDN Term
Short-wave diathermy treatment system, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5290 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 15 Pound FDA UDI

Category: Short-wave diathermy treatment system, professional

Auto*Therm 390 by Mettler Electronics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Short-wave diathermy treatment system, professional.

Cleared under the same submission

K042554 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 0e2fea2e-79fc-487a-85a3-5260b7d5b96b 38 fields · synced Jun 8, 2026