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FDA 510(k)

SERIES 8920 TROCAR SYSTEM

K-Number: K932441 · 1994-02-01

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1994-02-01
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SERIES 8920 TROCAR 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 1994-02-01 under 510(k) number K932441. 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 SERIES 8920 TROCAR SYSTEM?

SERIES 8920 TROCAR SYSTEM is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K932441.

When did SERIES 8920 TROCAR SYSTEM receive FDA 510(k) clearance?

SERIES 8920 TROCAR SYSTEM received FDA 510(k) clearance on 1994-02-01, under 510(k) number K932441.

Who is the listed applicant for SERIES 8920 TROCAR 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 SERIES 8920 TROCAR SYSTEM?

The FDA product code for SERIES 8920 TROCAR 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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