Cleared Traditional

K871782 - ULTRAVIOLET ALANINE AMINO-TRANS (UV-ALT...

K871782 is the FDA 510(k) clearance for ULTRAVIOLET ALANINE AMINO-TRANS (UV-ALT... by Biochemical Trade, Inc.. It is a Class 1 Chemistry device (product code CKA) cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K871782 · Biochemical Trade, Inc. · Chemistry device
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May 1987
Decision
20d
Days
Class 1
Risk

K871782 is an FDA 510(k) clearance for the ULTRAVIOLET ALANINE AMINO-TRANS (UV-ALT/UV-GPT). Classified as Nadh Oxidation/nad Reduction, Alt/sgpt (product code CKA), Class I - General Controls.

Submitted by Biochemical Trade, Inc. (Miami, US). The FDA issued a Cleared decision on May 26, 1987 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1030 - 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 Biochemical Trade, Inc. devices

Submission Details

510(k) Number K871782 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 1987
Decision Date May 26, 1987
Days to Decision 20 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 88d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code CKA Nadh Oxidation/nad Reduction, Alt/sgpt
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1030
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - CKA Nadh Oxidation/nad Reduction, Alt/sgpt

All 100
Devices cleared under the same product code (CKA) and FDA review panel - the closest regulatory comparables to K871782.
PYRIDOXAL-5-PHOSPHATE TABLETS
K874835 · Boehringer Mannheim Corp. · Jan 1988
MODIFIED ALT (GPT) REAGENT
K872483 · Trace Scientific , Ltd. · Aug 1987
BIOTROL ALT/TGP MONOREACTIF
K872830 · Biotrol, USA, Inc. · Aug 1987
ALANINE AMINOTRANSFERASE (ALT)/(GPT)
K870086 · Catachem, Inc. · Mar 1987
WAKO(TM) AUTOKIT GPT
K864850 · Wako Chemicals USA, Inc. · Jan 1987
ALANINE AMINO TRANSFERASE ALT/SGPT
K864906 · Tech-Co, Inc. · Dec 1986