Cleared Traditional

K801177 - ASO QUANTUM

K801177 is the FDA 510(k) clearance for ASO QUANTUM by Sclavo, Inc.. It is a Class 1 Microbiology device (product code GTQ) cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K801177 · Sclavo, Inc. · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1980
Decision
53d
Days
Class 1
Risk

K801177 is an FDA 510(k) clearance for the ASO QUANTUM, ANTISTREPTOLYSIN O TEST. Classified as Antistreptolysin - Titer/streptolysin O Reagent (product code GTQ), Class I - General Controls.

Submitted by Sclavo, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 8, 1980 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3720 - the FDA microbiology device 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 Sclavo, Inc. devices

Submission Details

510(k) Number K801177 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 16, 1980
Decision Date July 08, 1980
Days to Decision 53 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 102d · This submission: 53d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GTQ Antistreptolysin - Titer/streptolysin O Reagent
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.3720
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 - GTQ Antistreptolysin - Titer/streptolysin O Reagent

All 18
Devices cleared under the same product code (GTQ) and FDA review panel - the closest regulatory comparables to K801177.
SERIMM SURE ASO-CHEK CONTROL SERUM
K842839 · Analytical Products, Inc. · Aug 1984
ASO SURE
K820785 · Analytical Products, Inc. · Apr 1982
ASO SURE PLUS
K820786 · Analytical Products, Inc. · Apr 1982
RAPI/TEX ASO STANDARD SERUM
K800642 · Calbiochem-Behring Corp. · Apr 1980
ANTISTREPTOLYSIN (ASO) LATEX SLIDE TEST
K790831 · Icl Scientific · Jun 1979