Cleared Traditional

K914068 - ABBOTT QUICKSTART ASPARATE AMINOTRANSFE...

K914068 is the FDA 510(k) clearance for ABBOTT QUICKSTART ASPARATE AMINOTRANSFE... by Em Diagnostic Systems, Inc.. It is a Class 2 Chemistry device (product code CIT) cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K914068 · Em Diagnostic Systems, Inc. · Chemistry device
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Oct 1991
Decision
21d
Days
Class 2
Risk

K914068 is an FDA 510(k) clearance for the ABBOTT QUICKSTART ASPARATE AMINOTRANSFERASE TEST. Classified as Nadh Oxidation/nad Reduction, Ast/sgot (product code CIT), Class II - Special Controls.

Submitted by Em Diagnostic Systems, Inc. (Gibbstown, US). The FDA issued a Cleared decision on October 2, 1991 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1100 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Em Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K914068 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 1991
Decision Date October 02, 1991
Days to Decision 21 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
67d faster than avg
Panel avg: 88d · This submission: 21d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CIT Nadh Oxidation/nad Reduction, Ast/sgot
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1100
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CIT Nadh Oxidation/nad Reduction, Ast/sgot

All 104
Devices cleared under the same product code (CIT) and FDA review panel - the closest regulatory comparables to K914068.
SYNERMED AST/GOT REAGENT KIT
K915555 · Synermed, Inc. · Jan 1992
ABBOTT QUICKSTART SGOT, ITEM NUMBER: 5A42
K914463 · Em Diagnostic Systems, Inc. · Jan 1992
TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)
K914025 · Technicon Instruments Corp. · Nov 1991
COULTER DART AST (GOT) REAGENT
K905771 · Coulter Electronics, Inc. · Feb 1991
AST REAGENT
K903829 · Amresco, Inc. · Sep 1990
ASPARTATE AMINOTRANSFERASE TEST
K903197 · Em Diagnostic Systems, Inc. · Aug 1990