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FDA 510(k)

PATTON TRIPOL

K-Number: K012279 · 2002-04-30

ApplicantPatton Medical Corp.
Decision Date2002-04-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PATTON TRIPOL is the device name listed in this FDA 510(k) record. The listed applicant is Patton Medical Corp.. It received FDA 510(k) clearance on 2002-04-30 under 510(k) number K012279. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATTON TRIPOL?

PATTON TRIPOL is a medical device that received FDA 510(k) clearance on 2002-04-30. The listed applicant is Patton Medical Corp.. The 510(k) number is K012279.

When did PATTON TRIPOL receive FDA 510(k) clearance?

PATTON TRIPOL received FDA 510(k) clearance on 2002-04-30, under 510(k) number K012279.

Who is the listed applicant for PATTON TRIPOL?

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

What is the FDA product code for PATTON TRIPOL?

The FDA product code for PATTON TRIPOL is GEI.

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Other records listing Patton Medical Corp. 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.

K012150PATTON ENDO-BAGK991963PATTON SPECULUMK992324FUNNEL TROCAR

Related Devices (Code: GEI)

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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