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FDA 510(k)

ELECTROTHERM MODELS F&C18,14,78, F84

K-Number: K771999 · 1977-11-15

ApplicantElectromedics, Inc.
Decision Date1977-11-15
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELECTROTHERM MODELS F&C18,14,78, F84 is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1977-11-15 under 510(k) number K771999. 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 MODELS F&C18,14,78, F84?

ELECTROTHERM MODELS F&C18,14,78, F84 is a medical device that received FDA 510(k) clearance on 1977-11-15. The listed applicant is Electromedics, Inc.. The 510(k) number is K771999.

When did ELECTROTHERM MODELS F&C18,14,78, F84 receive FDA 510(k) clearance?

ELECTROTHERM MODELS F&C18,14,78, F84 received FDA 510(k) clearance on 1977-11-15, under 510(k) number K771999.

Who is the listed applicant for ELECTROTHERM MODELS F&C18,14,78, F84?

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 MODELS F&C18,14,78, F84?

The FDA product code for ELECTROTHERM MODELS F&C18,14,78, F84 is FLL.

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Related Devices (Code: FLL)

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.

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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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