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FDA 510(k)

FREDEIC BEAUSOCEIL

K-Number: K951551 · 1995-07-17

ApplicantPascal Mathieux
Decision Date1995-07-17
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FREDEIC BEAUSOCEIL is the device name listed in this FDA 510(k) record. The listed applicant is Pascal Mathieux. It received FDA 510(k) clearance on 1995-07-17 under 510(k) number K951551. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREDEIC BEAUSOCEIL?

FREDEIC BEAUSOCEIL is a medical device that received FDA 510(k) clearance on 1995-07-17. The listed applicant is Pascal Mathieux. The 510(k) number is K951551.

When did FREDEIC BEAUSOCEIL receive FDA 510(k) clearance?

FREDEIC BEAUSOCEIL received FDA 510(k) clearance on 1995-07-17, under 510(k) number K951551.

Who is the listed applicant for FREDEIC BEAUSOCEIL?

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

What is the FDA product code for FREDEIC BEAUSOCEIL?

The FDA product code for FREDEIC BEAUSOCEIL is HQY.

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Related Devices (Code: HQY)

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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