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FDA 510(k)

FOSSIL PARTNERS, L.P. (FOSSIL)

K-Number: K950374 · 1995-02-27

ApplicantStrasburger & Price, L.L.P.
Decision Date1995-02-27
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FOSSIL PARTNERS, L.P. (FOSSIL) is the device name listed in this FDA 510(k) record. The listed applicant is Strasburger & Price, L.L.P.. It received FDA 510(k) clearance on 1995-02-27 under 510(k) number K950374. 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 FOSSIL PARTNERS, L.P. (FOSSIL)?

FOSSIL PARTNERS, L.P. (FOSSIL) is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Strasburger & Price, L.L.P.. The 510(k) number is K950374.

When did FOSSIL PARTNERS, L.P. (FOSSIL) receive FDA 510(k) clearance?

FOSSIL PARTNERS, L.P. (FOSSIL) received FDA 510(k) clearance on 1995-02-27, under 510(k) number K950374.

Who is the listed applicant for FOSSIL PARTNERS, L.P. (FOSSIL)?

The FDA 510(k) record lists Strasburger & Price, L.L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOSSIL PARTNERS, L.P. (FOSSIL)?

The FDA product code for FOSSIL PARTNERS, L.P. (FOSSIL) is HQY.

Related Clinical Trials

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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