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FDA 510(k)

AFFIRM VPIII MICROBIAL IDENTIFICATION TEST

K-Number: K931374 · 1993-06-15

Decision Date1993-06-15
Product CodeMLA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AFFIRM VPIII MICROBIAL IDENTIFICATION TEST is the device name listed in this FDA 510(k) record. The listed applicant is Microprobe Corp.. It received FDA 510(k) clearance on 1993-06-15 under 510(k) number K931374. The device is classified under product code MLA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFFIRM VPIII MICROBIAL IDENTIFICATION TEST?

AFFIRM VPIII MICROBIAL IDENTIFICATION TEST is a medical device that received FDA 510(k) clearance on 1993-06-15. The listed applicant is Microprobe Corp.. The 510(k) number is K931374.

When did AFFIRM VPIII MICROBIAL IDENTIFICATION TEST receive FDA 510(k) clearance?

AFFIRM VPIII MICROBIAL IDENTIFICATION TEST received FDA 510(k) clearance on 1993-06-15, under 510(k) number K931374.

Who is the listed applicant for AFFIRM VPIII MICROBIAL IDENTIFICATION TEST?

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 VPIII MICROBIAL IDENTIFICATION TEST?

The FDA product code for AFFIRM VPIII MICROBIAL IDENTIFICATION TEST is MLA.

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.

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.

Related Devices (Code: MLA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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