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FDA 510(k)

ELECTROTHERM MODEL HT-1

K-Number: K771994 · 1977-11-02

ApplicantElectromedics, Inc.
Decision Date1977-11-02
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELECTROTHERM MODEL HT-1 is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1977-11-02 under 510(k) number K771994. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROTHERM MODEL HT-1?

ELECTROTHERM MODEL HT-1 is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is Electromedics, Inc.. The 510(k) number is K771994.

When did ELECTROTHERM MODEL HT-1 receive FDA 510(k) clearance?

ELECTROTHERM MODEL HT-1 received FDA 510(k) clearance on 1977-11-02, under 510(k) number K771994.

Who is the listed applicant for ELECTROTHERM MODEL HT-1?

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

What is the FDA product code for ELECTROTHERM MODEL HT-1?

The FDA product code for ELECTROTHERM MODEL HT-1 is FLL.

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Related Devices (Code: FLL)

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Official Source

View on FDA Database →

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

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