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FDA 510(k)

PREGNOPOST

K-Number: K821621 · 1982-07-21

ApplicantM.M. Wolfred, Ph.D.
Decision Date1982-07-21
Product CodeKDT
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PREGNOPOST is the device name listed in this FDA 510(k) record. The listed applicant is M.M. Wolfred, Ph.D.. It received FDA 510(k) clearance on 1982-07-21 under 510(k) number K821621. The device is classified under product code KDT. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREGNOPOST?

PREGNOPOST is a medical device that received FDA 510(k) clearance on 1982-07-21. The listed applicant is M.M. Wolfred, Ph.D.. The 510(k) number is K821621.

When did PREGNOPOST receive FDA 510(k) clearance?

PREGNOPOST received FDA 510(k) clearance on 1982-07-21, under 510(k) number K821621.

Who is the listed applicant for PREGNOPOST?

The FDA 510(k) record lists M.M. Wolfred, Ph.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREGNOPOST?

The FDA product code for PREGNOPOST is KDT.

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Related Devices (Code: KDT)

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.

K873593BIOSURE SPECIMEN COLLECTION CONTAINERBiosure, Inc.K862665NOVACYTE-UXsirius Medical, Inc.K834579BIOSPAL 2400SHospal Medical Corp.K834412PRESERV PVA FIXATIVE 15ML-FORMALIN PKPreventive Diagnostics Corp.K833660PRESERV PVA FIXATIVE -MALIN PACKPreventive Diagnostics Corp.K823773PROVIAL II #006-010-0201Dynatech Corp.

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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