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)

GGT QVET

K-Number: K942962 · 1994-12-07

Decision Date1994-12-07
Product CodeJQB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GGT QVET is the device name listed in this FDA 510(k) record. The listed applicant is Prisma Systems. It received FDA 510(k) clearance on 1994-12-07 under 510(k) number K942962. The device is classified under product code JQB. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GGT QVET?

GGT QVET is a medical device that received FDA 510(k) clearance on 1994-12-07. The listed applicant is Prisma Systems. The 510(k) number is K942962.

When did GGT QVET receive FDA 510(k) clearance?

GGT QVET received FDA 510(k) clearance on 1994-12-07, under 510(k) number K942962.

Who is the listed applicant for GGT QVET?

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

What is the FDA product code for GGT QVET?

The FDA product code for GGT QVET is JQB.

Other records listing Prisma Systems 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.

View all 27 devices →

Related Devices (Code: JQB)

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.

↑