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FDA 510(k)

ENDOSCOPIC RETRACTOR

K-Number: K931092 · 1993-04-30

ApplicantL.A.S.E.R., Inc.
Decision Date1993-04-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is L.A.S.E.R., Inc.. It received FDA 510(k) clearance on 1993-04-30 under 510(k) number K931092. 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 ENDOSCOPIC RETRACTOR?

ENDOSCOPIC RETRACTOR is a medical device that received FDA 510(k) clearance on 1993-04-30. The listed applicant is L.A.S.E.R., Inc.. The 510(k) number is K931092.

When did ENDOSCOPIC RETRACTOR receive FDA 510(k) clearance?

ENDOSCOPIC RETRACTOR received FDA 510(k) clearance on 1993-04-30, under 510(k) number K931092.

Who is the listed applicant for ENDOSCOPIC RETRACTOR?

The FDA 510(k) record lists L.A.S.E.R., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC RETRACTOR?

The FDA product code for ENDOSCOPIC RETRACTOR is GCJ.

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Other records listing L.A.S.E.R., Inc. as applicant

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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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