Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA

K-Number: K922457 · 1992-09-25

Decision Date1992-09-25
Product CodeMJK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA 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 K922457. The device is classified under product code MJK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA?

AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA 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 K922457.

When did AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA receive FDA 510(k) clearance?

AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA received FDA 510(k) clearance on 1992-09-25, under 510(k) number K922457.

Who is the listed applicant for AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA?

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 MICROBIAL ID TEST FOR TRICHOMONAS VAGINA?

The FDA product code for AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA is MJK.

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.

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.

↑