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FDA 510(k)

POLYPERF / POLYPERF SAFE

K-Number: K063631 · 2007-10-05

Decision Date2007-10-05
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POLYPERF / POLYPERF SAFE is the device name listed in this FDA 510(k) record. The listed applicant is Laboratoires Perouse. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K063631. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYPERF / POLYPERF SAFE?

POLYPERF / POLYPERF SAFE is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Laboratoires Perouse. The 510(k) number is K063631.

When did POLYPERF / POLYPERF SAFE receive FDA 510(k) clearance?

POLYPERF / POLYPERF SAFE received FDA 510(k) clearance on 2007-10-05, under 510(k) number K063631.

Who is the listed applicant for POLYPERF / POLYPERF SAFE?

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

What is the FDA product code for POLYPERF / POLYPERF SAFE?

The FDA product code for POLYPERF / POLYPERF SAFE is FPA.

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: FPA)

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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