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FDA 510(k)

WINTER HEAD DRESSING

K-Number: K801458 · 1980-07-28

ApplicantSteridyne Corp.
Decision Date1980-07-28
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WINTER HEAD DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Steridyne Corp.. It received FDA 510(k) clearance on 1980-07-28 under 510(k) number K801458. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINTER HEAD DRESSING?

WINTER HEAD DRESSING is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Steridyne Corp.. The 510(k) number is K801458.

When did WINTER HEAD DRESSING receive FDA 510(k) clearance?

WINTER HEAD DRESSING received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801458.

Who is the listed applicant for WINTER HEAD DRESSING?

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

What is the FDA product code for WINTER HEAD DRESSING?

The FDA product code for WINTER HEAD DRESSING is FQM.

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Other records listing Steridyne Corp. 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.

K925352CLEAN CUFF BLOOD PRESSURE CUFF LINERK911843ZERO-G(TM) GEL/FOAM MATTRESS TOPPERK911269MERCURY AND GLASS FEVER THERMOMETERK842120ZERO-GK821314FEVER METER

Related Devices (Code: FQM)

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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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