Cleared Traditional

K963551 - BIO-CSF LIQUID CONTROL LEVEL 1 AND 2

K963551 is the FDA 510(k) clearance for BIO-CSF LIQUID CONTROL LEVEL 1 AND 2 by Biocell Laboratories, Inc.. It is a Class 1 Chemistry device (product code JJX) cleared through the Traditional 510(k) pathway after a 32-day FDA review.

K963551 · Biocell Laboratories, Inc. · Chemistry device
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Oct 1996
Decision
32d
Days
Class 1
Risk

K963551 is an FDA 510(k) clearance for the BIO-CSF LIQUID CONTROL LEVEL 1 AND 2. Classified as Single (specified) Analyte Controls (assayed And Unassayed) (product code JJX), Class I - General Controls.

Submitted by Biocell Laboratories, Inc. (Rancho Dominguez, US). The FDA issued a Cleared decision on October 7, 1996 after a review of 32 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1660 - 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 Biocell Laboratories, Inc. devices

Submission Details

510(k) Number K963551 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 05, 1996
Decision Date October 07, 1996
Days to Decision 32 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 88d · This submission: 32d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJX Single (specified) Analyte Controls (assayed And Unassayed)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1660
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 - JJX Single (specified) Analyte Controls (assayed And Unassayed)

All 376
Devices cleared under the same product code (JJX) and FDA review panel - the closest regulatory comparables to K963551.
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PROSTATE SPECIFIC ANTIGEN (RSA) CONTROL MODDULE (PSACM)
K962975 · Diagnostic Products Corp. · Aug 1996