Cleared Traditional

K961293 - QUIKCHECK UNASSAYED CHEMISTRY CONTROL LEVELS 1 & 2

K961293 is an FDA 510(k) clearance for QUIKCHECK UNASSAYED CHEMISTRY CONTROL L..., manufactured by Consolidated Technologies, Inc.. The device is a Class 1 Chemistry device with product code JJY cleared through the Traditional 510(k) pathway after a 28-day FDA review.

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May 1996
Decision
28d
Days
Class 1
Risk

K961293 is an FDA 510(k) clearance for the QUIKCHECK UNASSAYED CHEMISTRY CONTROL LEVELS 1 & 2. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by Consolidated Technologies, Inc. (Austin, US). The FDA issued a Cleared decision on May 2, 1996 after a review of 28 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 Consolidated Technologies, Inc. devices

FDA 510(k) Submission Details - K961293

510(k) Number K961293 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 04, 1996
Decision Date May 02, 1996
Days to Decision 28 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
60d faster than avg
Panel avg: 88d · This submission: 28d
Pathway characteristics
Predicate-based equivalence.

JJY Device Classification - Class 1, General Controls

Product Code JJY Multi-analyte Controls, All Kinds (assayed)
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 - JJY Multi-analyte Controls, All Kinds (assayed)

All 594
Devices cleared under the same product code (JJY) and FDA review panel - the closest regulatory comparables to K961293.
ELECSYS PRECICONTROL CARDIAC
K962575 · Boehringer Mannheim Corp. · Jul 1996
DOCUMENT AMMONIA, ETHANOL, LACTATE ASSAYED CONTROL
K962630 · Casco Standards · Jul 1996
CHEM-CHEX STAT
K961195 · Streck Laboratories, Inc. · May 1996
AQUEOUS ETHANOL/AMMONIA CONTROL LEVEL 1, 2, & 3
K955690 · Clinical Controls, Inc. · Apr 1996
SERUM VOLATILES CONTROL LEVEL 1 & 2
K955691 · Clinical Controls, Inc. · Apr 1996
IMMUNOLOGY CONTROL
K960824 · Medical Analysis Systems, Inc. · Apr 1996