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FDA 510(k)

LM-1Z ZOOM SCOPE

K-Number: K902313 · 1990-09-04

ApplicantLeisegang Medical, Inc.
Decision Date1990-09-04
Product CodeHEX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LM-1Z ZOOM SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Leisegang Medical, Inc.. It received FDA 510(k) clearance on 1990-09-04 under 510(k) number K902313. The device is classified under product code HEX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LM-1Z ZOOM SCOPE?

LM-1Z ZOOM SCOPE is a medical device that received FDA 510(k) clearance on 1990-09-04. The listed applicant is Leisegang Medical, Inc.. The 510(k) number is K902313.

When did LM-1Z ZOOM SCOPE receive FDA 510(k) clearance?

LM-1Z ZOOM SCOPE received FDA 510(k) clearance on 1990-09-04, under 510(k) number K902313.

Who is the listed applicant for LM-1Z ZOOM SCOPE?

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

What is the FDA product code for LM-1Z ZOOM SCOPE?

The FDA product code for LM-1Z ZOOM SCOPE is HEX.

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Other records listing Leisegang Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K990043SMOOTHLASE ALEXANDRITE LASER SYSTEMK940094COLPOSCOPES AND ACCESSORIESK924134LEISEGANG LAPAROSCOPIC IRRIGATION SYSTEM/ACCESSK920217MAX-E-VACK914201LM- LAP 10 HIGH FLOW INSUFFLATORK912789LM-100/200LOW FLOW INSUFFLATOR

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Related Devices (Code: HEX)

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K233043Smart Scope® CXPeriwinkle Technologies Pvt., Ltd.K190187Gynescope SystemIllumigyn , Ltd.K182764Biop Digital ColposcopeBiop Medical , Ltd.K181034Pocket Colposcope SystemHadleigh Health Technologies, LLCK170446LT-300 SD Digital Video ColposcopeLutech Industries, Inc.K161871EVA (Enhanced Visual Assessment) SystemMobileodt , Ltd.

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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