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FDA 510(k)

AFFIRM VP SAMPLE COLLECTION SET

K-Number: K920536 · 1992-07-30

ApplicantMicroprobe Corp.
Decision Date1992-07-30
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AFFIRM VP SAMPLE COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Microprobe Corp.. It received FDA 510(k) clearance on 1992-07-30 under 510(k) number K920536. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFFIRM VP SAMPLE COLLECTION SET?

AFFIRM VP SAMPLE COLLECTION SET is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Microprobe Corp.. The 510(k) number is K920536.

When did AFFIRM VP SAMPLE COLLECTION SET receive FDA 510(k) clearance?

AFFIRM VP SAMPLE COLLECTION SET received FDA 510(k) clearance on 1992-07-30, under 510(k) number K920536.

Who is the listed applicant for AFFIRM VP SAMPLE COLLECTION SET?

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 SAMPLE COLLECTION SET?

The FDA product code for AFFIRM VP SAMPLE COLLECTION SET is LIO.

Related Clinical Trials

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.

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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 VAGINAK923133AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALISK923268AFFIRM PROCESSOR

Related Devices (Code: LIO)

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.

K222613ARX Liquid Amies Collection & Transport SystemArx Sciences, Inc.K131630PURITAN AMIES MEDIUM COLLECTION AND TRANSPORT SYSTEMPuritan Medical Products, LLCK120846TRANSPORT CULTURE MEDIUM DEVICEPuritan Medical Products, LLCK103805MEDICAL WIRE & EQUIPMENT S-TRANSWAB (OR SIGMA-TRANSWAB) LIQUID AMIES COLLECTION AND TRANSPORT DEVICEMedical Wire & Equipment Company (Bath), Ltd.K082472VIROCULT, MODEL MW950Medical Wire & Equipment Company (Bath), Ltd.K070062COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USEDiesse Diagnostica Senese S.P.A.

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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