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)

PRE-VAP CAPS

K-Number: K810394 · 1981-03-06

Decision Date1981-03-06
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRE-VAP CAPS is the device name listed in this FDA 510(k) record. The listed applicant is Sherman Boosalis. It received FDA 510(k) clearance on 1981-03-06 under 510(k) number K810394. The device is classified under product code JJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-VAP CAPS?

PRE-VAP CAPS is a medical device that received FDA 510(k) clearance on 1981-03-06. The listed applicant is Sherman Boosalis. The 510(k) number is K810394.

When did PRE-VAP CAPS receive FDA 510(k) clearance?

PRE-VAP CAPS received FDA 510(k) clearance on 1981-03-06, under 510(k) number K810394.

Who is the listed applicant for PRE-VAP CAPS?

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

What is the FDA product code for PRE-VAP CAPS?

The FDA product code for PRE-VAP CAPS is JJC.

Related Devices (Code: JJC)

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.

↑