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FDA 510(k)

DERMALEX OR NATRAWOOL SKIN PRESSURE PROT

K-Number: K801195 · 1980-06-09

Decision Date1980-06-09
Product CodeFMP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMALEX OR NATRAWOOL SKIN PRESSURE PROT is the device name listed in this FDA 510(k) record. The listed applicant is Stock Wild & Co.. It received FDA 510(k) clearance on 1980-06-09 under 510(k) number K801195. The device is classified under product code FMP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMALEX OR NATRAWOOL SKIN PRESSURE PROT?

DERMALEX OR NATRAWOOL SKIN PRESSURE PROT is a medical device that received FDA 510(k) clearance on 1980-06-09. The listed applicant is Stock Wild & Co.. The 510(k) number is K801195.

When did DERMALEX OR NATRAWOOL SKIN PRESSURE PROT receive FDA 510(k) clearance?

DERMALEX OR NATRAWOOL SKIN PRESSURE PROT received FDA 510(k) clearance on 1980-06-09, under 510(k) number K801195.

Who is the listed applicant for DERMALEX OR NATRAWOOL SKIN PRESSURE PROT?

The FDA 510(k) record lists Stock Wild & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERMALEX OR NATRAWOOL SKIN PRESSURE PROT?

The FDA product code for DERMALEX OR NATRAWOOL SKIN PRESSURE PROT is FMP.

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: FMP)

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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