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FDA 510(k)

AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS

K-Number: K923133 · 1992-09-25

ApplicantMicroprobe Corp.
Decision Date1992-09-25
Product CodeMJM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS is the device name listed in this FDA 510(k) record. The listed applicant is Microprobe Corp.. It received FDA 510(k) clearance on 1992-09-25 under 510(k) number K923133. The device is classified under product code MJM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS?

AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS is a medical device that received FDA 510(k) clearance on 1992-09-25. The listed applicant is Microprobe Corp.. The 510(k) number is K923133.

When did AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS receive FDA 510(k) clearance?

AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS received FDA 510(k) clearance on 1992-09-25, under 510(k) number K923133.

Who is the listed applicant for AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS?

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

What is the FDA product code for AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS?

The FDA product code for AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS is MJM.

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Other records listing Microprobe Corp. 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.

K931151AFFIRM(TM) VPIII MICROBIAL IDENT TEST FOR CANDIDAK931374AFFIRM VPIII MICROBIAL IDENTIFICATION TESTK922457AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINAK920536AFFIRM VP SAMPLE COLLECTION SETK923268AFFIRM PROCESSOR

Related Devices (Code: MJM)

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.

K964015INDICARD TESTLitmus Concepts, Inc.

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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