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FDA 510(k)

MATELAS COQUILLE LATTREDE TASSIGNY

K-Number: K811547 · 1981-06-18

ApplicantFirn-France
Decision Date1981-06-18
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MATELAS COQUILLE LATTREDE TASSIGNY is the device name listed in this FDA 510(k) record. The listed applicant is Firn-France. It received FDA 510(k) clearance on 1981-06-18 under 510(k) number K811547. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATELAS COQUILLE LATTREDE TASSIGNY?

MATELAS COQUILLE LATTREDE TASSIGNY is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Firn-France. The 510(k) number is K811547.

When did MATELAS COQUILLE LATTREDE TASSIGNY receive FDA 510(k) clearance?

MATELAS COQUILLE LATTREDE TASSIGNY received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811547.

Who is the listed applicant for MATELAS COQUILLE LATTREDE TASSIGNY?

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

What is the FDA product code for MATELAS COQUILLE LATTREDE TASSIGNY?

The FDA product code for MATELAS COQUILLE LATTREDE TASSIGNY is FPP.

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Related Devices (Code: FPP)

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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