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FDA 510(k)

COLPOSTAR V-6

K-Number: K871683 · 1987-08-05

ApplicantWallach Surgical Devices, Inc.
Decision Date1987-08-05
Product CodeHEX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COLPOSTAR V-6 is the device name listed in this FDA 510(k) record. The listed applicant is Wallach Surgical Devices, Inc.. It received FDA 510(k) clearance on 1987-08-05 under 510(k) number K871683. 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 COLPOSTAR V-6?

COLPOSTAR V-6 is a medical device that received FDA 510(k) clearance on 1987-08-05. The listed applicant is Wallach Surgical Devices, Inc.. The 510(k) number is K871683.

When did COLPOSTAR V-6 receive FDA 510(k) clearance?

COLPOSTAR V-6 received FDA 510(k) clearance on 1987-08-05, under 510(k) number K871683.

Who is the listed applicant for COLPOSTAR V-6?

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

What is the FDA product code for COLPOSTAR V-6?

The FDA product code for COLPOSTAR V-6 is HEX.

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Other records listing Wallach Surgical Devices, 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.

K021224ENDOCERVICAL BLOCK NEEDLEK020711WALLACH LOOP ELECTRODEK000768WALLACH QUANTUM 500 ELECTROSURGICAL GENERATORK992736WALLACH'S ULTIMATE REUSABLE, PLASTIC VAGINAL SPECULUMK991669PMS 750 FINGERSWITCHK983840WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR (PROPOSED)

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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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