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FDA 510(k)

ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER

K-Number: K875381 · 1988-05-03

Decision Date1988-05-03
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER is the device name listed in this FDA 510(k) record. The listed applicant is Ford Laboratories, Inc.. It received FDA 510(k) clearance on 1988-05-03 under 510(k) number K875381. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER?

ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER is a medical device that received FDA 510(k) clearance on 1988-05-03. The listed applicant is Ford Laboratories, Inc.. The 510(k) number is K875381.

When did ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER receive FDA 510(k) clearance?

ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER received FDA 510(k) clearance on 1988-05-03, under 510(k) number K875381.

Who is the listed applicant for ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER?

The FDA 510(k) record lists Ford Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER?

The FDA product code for ULTRASOUND DIATHERMY UNIT ULTRASOUND HEATER is IMI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: IMI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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