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FDA 510(k)

HM-0690 COLPOSCOPE

K-Number: K932896 · 1994-03-23

ApplicantHill-Med, Inc.
Decision Date1994-03-23
Product CodeHEX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HM-0690 COLPOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Med, Inc.. It received FDA 510(k) clearance on 1994-03-23 under 510(k) number K932896. 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 HM-0690 COLPOSCOPE?

HM-0690 COLPOSCOPE is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is Hill-Med, Inc.. The 510(k) number is K932896.

When did HM-0690 COLPOSCOPE receive FDA 510(k) clearance?

HM-0690 COLPOSCOPE received FDA 510(k) clearance on 1994-03-23, under 510(k) number K932896.

Who is the listed applicant for HM-0690 COLPOSCOPE?

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

What is the FDA product code for HM-0690 COLPOSCOPE?

The FDA product code for HM-0690 COLPOSCOPE is HEX.

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Other records listing Hill-Med, Inc. as applicant

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Related Devices (Code: HEX)

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.

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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