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FDA 510(k)

PATTON ENDO-BAG

K-Number: K012150 · 2001-09-20

ApplicantPatton Medical Corp.
Decision Date2001-09-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PATTON ENDO-BAG 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 2001-09-20 under 510(k) number K012150. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATTON ENDO-BAG?

PATTON ENDO-BAG is a medical device that received FDA 510(k) clearance on 2001-09-20. The listed applicant is Patton Medical Corp.. The 510(k) number is K012150.

When did PATTON ENDO-BAG receive FDA 510(k) clearance?

PATTON ENDO-BAG received FDA 510(k) clearance on 2001-09-20, under 510(k) number K012150.

Who is the listed applicant for PATTON ENDO-BAG?

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 ENDO-BAG?

The FDA product code for PATTON ENDO-BAG is GCJ.

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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.

K012279PATTON TRIPOLK991963PATTON SPECULUMK992324FUNNEL TROCAR

Related Devices (Code: GCJ)

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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