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FDA 510(k)

MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM

K-Number: K863274 · 1986-09-02

ApplicantMartin Medical
Decision Date1986-09-02
Product CodeHIB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM is the device name listed in this FDA 510(k) record. The listed applicant is Martin Medical. It received FDA 510(k) clearance on 1986-09-02 under 510(k) number K863274. The device is classified under product code HIB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM?

MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM is a medical device that received FDA 510(k) clearance on 1986-09-02. The listed applicant is Martin Medical. The 510(k) number is K863274.

When did MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM receive FDA 510(k) clearance?

MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM received FDA 510(k) clearance on 1986-09-02, under 510(k) number K863274.

Who is the listed applicant for MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM?

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

What is the FDA product code for MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM?

The FDA product code for MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM is HIB.

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Other records listing Martin Medical 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.

K873723PLASTER VACUUM, 230V MODEL NO. 4183-161K873721PLASTER VACUUM, 115V MODEL NO. 4183-160K873722PEDESTAL WALKING HEEL PRODUCT NO. 4183-133K873716ADULT WALKING HEEL PRODUCT NO. 4183-130K873719CAST CUTTER, 115V MODEL NO. 4183-106K873720CAST CUTTER, 230V MODEL NO. 4183-107

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Related Devices (Code: HIB)

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.

K252208JFord Speculum Sleeve™Ford Medtech, LLCK130046CLEARSPEC SINGLE USE VAGINAL SPECULUMClearspec, LLCK120743SPECULUM, VAGINAL, NONMETALWelch Allyn, Inc.K110766KOLPLUX SYSTEMKolplast CI LtdaK092870NON-STERILE DISPOSABLE VAGINAL SPECULUMKunshan Deyi Plastic Co., Ltd.K091937OFFICE-SPEC DISPOSABLE SIDE-OPENING SPECULUMObp Corporation

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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