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FDA 510(k)

PATTON LAPAROSCOPIC CATHETER INTRODUCER SET

K-Number: K940265 · 1995-09-28

Decision Date1995-09-28
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PATTON LAPAROSCOPIC CATHETER INTRODUCER SET is the device name listed in this FDA 510(k) record. The listed applicant is Cook Urological, Inc.. It received FDA 510(k) clearance on 1995-09-28 under 510(k) number K940265. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATTON LAPAROSCOPIC CATHETER INTRODUCER SET?

PATTON LAPAROSCOPIC CATHETER INTRODUCER SET is a medical device that received FDA 510(k) clearance on 1995-09-28. The listed applicant is Cook Urological, Inc.. The 510(k) number is K940265.

When did PATTON LAPAROSCOPIC CATHETER INTRODUCER SET receive FDA 510(k) clearance?

PATTON LAPAROSCOPIC CATHETER INTRODUCER SET received FDA 510(k) clearance on 1995-09-28, under 510(k) number K940265.

Who is the listed applicant for PATTON LAPAROSCOPIC CATHETER INTRODUCER SET?

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

What is the FDA product code for PATTON LAPAROSCOPIC CATHETER INTRODUCER SET?

The FDA product code for PATTON LAPAROSCOPIC CATHETER INTRODUCER SET is HET.

Related Clinical Trials

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.

Other records listing Cook Urological, 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.

View all 104 devices →

Related Devices (Code: HET)

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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