Cleared Traditional

K895967 - FASTEC 901 AGGLUTINATION PATTERN READER

K895967 is an FDA 510(k) clearance for FASTEC 901 AGGLUTINATION PATTERN READER, manufactured by Schiff & Co.. The device is a Class 1 Microbiology device with product code JJQ cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K895967 · Schiff & Co. · Microbiology device
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Oct 1989
Decision
18d
Days
Class 1
Risk

K895967 is an FDA 510(k) clearance for the FASTEC 901 AGGLUTINATION PATTERN READER. Classified as Colorimeter, Photometer, Spectrophotometer For Clinical Use (product code JJQ), Class I - General Controls.

Submitted by Schiff & Co. (West Cadwell, US). The FDA issued a Cleared decision on October 30, 1989 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 862.2300 - 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 Schiff & Co. devices

FDA 510(k) Submission Details - K895967

510(k) Number K895967 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 12, 1989
Decision Date October 30, 1989
Days to Decision 18 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
84d faster than avg
Panel avg: 102d · This submission: 18d
Pathway characteristics
Predicate-based equivalence.

JJQ Device Classification - Class 1, General Controls

Product Code JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2300
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 - JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

All 163
Devices cleared under the same product code (JJQ) and FDA review panel - the closest regulatory comparables to K895967.
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K894687 · Dynatech Laboratories, Inc. · Aug 1989
QUIDEL REFLECTANCE ANALYZER
K893738 · Quidel Corp. · Aug 1989