Cleared Traditional

LVM QUALITY CONTROL SERUM (K902235) - FDA 510(k) Clearance

Class I Chemistry device.

K902235 · Ciba Corning Diagnostics Corp. · Chemistry device
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Jul 1990
Decision
61d
Days
Class 1
Risk

K902235 is an FDA 510(k) clearance for the LVM QUALITY CONTROL SERUM. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by Ciba Corning Diagnostics Corp. (East Walpole, US). The FDA issued a Cleared decision on July 17, 1990 after a review of 61 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 Ciba Corning Diagnostics Corp. devices

Submission Details

510(k) Number K902235 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 17, 1990
Decision Date July 17, 1990
Days to Decision 61 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 88d · This submission: 61d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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 222
Devices cleared under the same product code (JJY) and FDA review panel - the closest regulatory comparables to K902235.
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PRECINORM(R) IM NORMAL IMMUNOASSAY CONTROL SERUM
K902536 · Boehringer Mannheim Corp. · Jul 1990
PRECIPATH(R) IM ABNORMAL IMMUNASSAY CONTROL SERUM
K902573 · Boehringer Mannheim Corp. · Jul 1990
LIG/TDM A, B, C
K901212 · Ciba Corning Diagnostics Corp. · May 1990