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FDA 510(k)

PPMI-(XXX) AND PPMO-(XXX)

K-Number: K953231 · 1995-09-07

Decision Date1995-09-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PPMI-(XXX) AND PPMO-(XXX) is the device name listed in this FDA 510(k) record. The listed applicant is Patriot Products, Inc.. It received FDA 510(k) clearance on 1995-09-07 under 510(k) number K953231. 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 PPMI-(XXX) AND PPMO-(XXX)?

PPMI-(XXX) AND PPMO-(XXX) is a medical device that received FDA 510(k) clearance on 1995-09-07. The listed applicant is Patriot Products, Inc.. The 510(k) number is K953231.

When did PPMI-(XXX) AND PPMO-(XXX) receive FDA 510(k) clearance?

PPMI-(XXX) AND PPMO-(XXX) received FDA 510(k) clearance on 1995-09-07, under 510(k) number K953231.

Who is the listed applicant for PPMI-(XXX) AND PPMO-(XXX)?

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

What is the FDA product code for PPMI-(XXX) AND PPMO-(XXX)?

The FDA product code for PPMI-(XXX) AND PPMO-(XXX) is FPA.

Other records listing Patriot Products, Inc. as applicant

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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