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FDA 510(k)

LAPAROSCOPY OPTICS

K-Number: K932321 · 1993-12-09

ApplicantMedline Industries, Inc.
Decision Date1993-12-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPY OPTICS is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1993-12-09 under 510(k) number K932321. 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 LAPAROSCOPY OPTICS?

LAPAROSCOPY OPTICS is a medical device that received FDA 510(k) clearance on 1993-12-09. The listed applicant is Medline Industries, Inc.. The 510(k) number is K932321.

When did LAPAROSCOPY OPTICS receive FDA 510(k) clearance?

LAPAROSCOPY OPTICS received FDA 510(k) clearance on 1993-12-09, under 510(k) number K932321.

Who is the listed applicant for LAPAROSCOPY OPTICS?

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

What is the FDA product code for LAPAROSCOPY OPTICS?

The FDA product code for LAPAROSCOPY OPTICS is GCJ.

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Related Devices (Code: 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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