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FDA 510(k)

OPEN LAPAROSCOPY TROCAR CONE SYSTEM

K-Number: K941222 · 1995-01-18

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1995-01-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OPEN LAPAROSCOPY TROCAR CONE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1995-01-18 under 510(k) number K941222. 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 OPEN LAPAROSCOPY TROCAR CONE SYSTEM?

OPEN LAPAROSCOPY TROCAR CONE SYSTEM is a medical device that received FDA 510(k) clearance on 1995-01-18. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K941222.

When did OPEN LAPAROSCOPY TROCAR CONE SYSTEM receive FDA 510(k) clearance?

OPEN LAPAROSCOPY TROCAR CONE SYSTEM received FDA 510(k) clearance on 1995-01-18, under 510(k) number K941222.

Who is the listed applicant for OPEN LAPAROSCOPY TROCAR CONE SYSTEM?

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

What is the FDA product code for OPEN LAPAROSCOPY TROCAR CONE SYSTEM?

The FDA product code for OPEN LAPAROSCOPY TROCAR CONE SYSTEM is GCJ.

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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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