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FDA 510(k)

PC-BEADS POSTCOITAL TEST

K-Number: K902995 · 1991-01-31

ApplicantMicroscopy Research Innovations
Decision Date1991-01-31
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PC-BEADS POSTCOITAL TEST is the device name listed in this FDA 510(k) record. The listed applicant is Microscopy Research Innovations. It received FDA 510(k) clearance on 1991-01-31 under 510(k) number K902995. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PC-BEADS POSTCOITAL TEST?

PC-BEADS POSTCOITAL TEST is a medical device that received FDA 510(k) clearance on 1991-01-31. The listed applicant is Microscopy Research Innovations. The 510(k) number is K902995.

When did PC-BEADS POSTCOITAL TEST receive FDA 510(k) clearance?

PC-BEADS POSTCOITAL TEST received FDA 510(k) clearance on 1991-01-31, under 510(k) number K902995.

Who is the listed applicant for PC-BEADS POSTCOITAL TEST?

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

What is the FDA product code for PC-BEADS POSTCOITAL TEST?

The FDA product code for PC-BEADS POSTCOITAL TEST is HHT.

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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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