FDA 510(k)

AST QVET

K-Number: K944102 · 1994-12-13

Decision Date1994-12-13

Product CodeCIT

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

AST 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 1994-12-13 under 510(k) number K944102. The device is classified under product code CIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AST QVET?

AST QVET is a medical device that received FDA 510(k) clearance on 1994-12-13. The listed applicant is Prisma Systems. The 510(k) number is K944102.

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

AST QVET received FDA 510(k) clearance on 1994-12-13, under 510(k) number K944102.

Who is the listed applicant for AST 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 AST QVET?

The FDA product code for AST QVET is CIT.

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.

K950177CK QVET K943027CHOLESTEROL QVET K943001MAGNESIUM QVET K942964LACTATE DEHYDROGENASE QVET K943042BUN QVET K942997ALKALINE PHOSPHATASE (ALKP) QVET

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Related Devices (Code: CIT)

K093883AST/GOT 4+1 SL, AST/GOT 4+1 SL, ELICAL 2, ELITROL I, ELITROL II, MODEL ASSL-0250, ASSL-0455, CALI-0580, CONT-0080, CONT-Seppim S.A.S.K080485ASPARTATE AMINO TRANSFERASE (AST/SGOT) TEST SYSTEM, ASAT (GOT) FSDiasys Diagnostics Systems GmbH K071525ACTIVATED ASPARTATE AMINOTRANSFERASEAbbott Laboratories K071580AST/GOT (IFCC), PYRIDOXAL PHOSPHATE, ECAL, NORTROL AND ABTROLThermofisher Scientific OY K071211COBAS C 111 ANALYZERRoche Diagnostics K060318HEPATIC ENZYMES ON ABX PENTRA 400 CLINICAL CHEMISTRY ANALYZERHoriba Abx

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.