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FDA 510(k)

PHILIPPE CHARRIOL

K-Number: K950193 · 1995-02-24

ApplicantPhilippe Charriol Dist., Inc.
Decision Date1995-02-24
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHILIPPE CHARRIOL is the device name listed in this FDA 510(k) record. The listed applicant is Philippe Charriol Dist., Inc.. It received FDA 510(k) clearance on 1995-02-24 under 510(k) number K950193. 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 PHILIPPE CHARRIOL?

PHILIPPE CHARRIOL is a medical device that received FDA 510(k) clearance on 1995-02-24. The listed applicant is Philippe Charriol Dist., Inc.. The 510(k) number is K950193.

When did PHILIPPE CHARRIOL receive FDA 510(k) clearance?

PHILIPPE CHARRIOL received FDA 510(k) clearance on 1995-02-24, under 510(k) number K950193.

Who is the listed applicant for PHILIPPE CHARRIOL?

The FDA 510(k) record lists Philippe Charriol Dist., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPPE CHARRIOL?

The FDA product code for PHILIPPE CHARRIOL is HQY.

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Related Devices (Code: HQY)

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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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