FDA 510(k)

CASSETTE SYSTEM FOR STORZ

K-Number: K942945 · 1994-12-05

ApplicantSurgin Surgical Instrumentation, Inc.

Decision Date1994-12-05

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

CASSETTE SYSTEM FOR STORZ is the device name listed in this FDA 510(k) record. The listed applicant is Surgin Surgical Instrumentation, Inc.. It received FDA 510(k) clearance on 1994-12-05 under 510(k) number K942945. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CASSETTE SYSTEM FOR STORZ?

CASSETTE SYSTEM FOR STORZ is a medical device that received FDA 510(k) clearance on 1994-12-05. The listed applicant is Surgin Surgical Instrumentation, Inc.. The 510(k) number is K942945.

When did CASSETTE SYSTEM FOR STORZ receive FDA 510(k) clearance?

CASSETTE SYSTEM FOR STORZ received FDA 510(k) clearance on 1994-12-05, under 510(k) number K942945.

Who is the listed applicant for CASSETTE SYSTEM FOR STORZ?

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

What is the FDA product code for CASSETTE SYSTEM FOR STORZ?

The FDA product code for CASSETTE SYSTEM FOR STORZ is HQC.

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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.