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FDA 510(k)

FUNGUS FIGHTER INSOLES

K-Number: K780719 · 1978-10-10

ApplicantCombe, Inc.
Decision Date1978-10-10
Product CodeKYS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FUNGUS FIGHTER INSOLES is the device name listed in this FDA 510(k) record. The listed applicant is Combe, Inc.. It received FDA 510(k) clearance on 1978-10-10 under 510(k) number K780719. The device is classified under product code KYS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUNGUS FIGHTER INSOLES?

FUNGUS FIGHTER INSOLES is a medical device that received FDA 510(k) clearance on 1978-10-10. The listed applicant is Combe, Inc.. The 510(k) number is K780719.

When did FUNGUS FIGHTER INSOLES receive FDA 510(k) clearance?

FUNGUS FIGHTER INSOLES received FDA 510(k) clearance on 1978-10-10, under 510(k) number K780719.

Who is the listed applicant for FUNGUS FIGHTER INSOLES?

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

What is the FDA product code for FUNGUS FIGHTER INSOLES?

The FDA product code for FUNGUS FIGHTER INSOLES is KYS.

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Other records listing Combe, Inc. as applicant

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.

K942203OTC DENTURE CLEANSERK925259CFR MONOGRAPHK863375SEA-BONDK770413CUSHIONS, DENTURE ADHESIVE, ALL-DAYK770175SEA-BOND ADHEVISE DENTURE CUSHIONS

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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