Cleared Traditional

K870036 - BAYER HEALTHCARE RAPIDQC PLUS

K870036 is an FDA 510(k) clearance for BAYER HEALTHCARE RAPIDQC PLUS, manufactured by Ciba Corning Diagnostics Corp.. The device is a Class 1 Chemistry device with product code JJS cleared through the Traditional 510(k) pathway after a 9-day FDA review.

K870036 · Ciba Corning Diagnostics Corp. · Chemistry device
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Jan 1987
Decision
9d
Days
Class 1
Risk

K870036 is an FDA 510(k) clearance for the BAYER HEALTHCARE RAPIDQC PLUS. Classified as Controls For Blood-gases, (assayed And Unassayed) (product code JJS), Class I - General Controls.

Submitted by Ciba Corning Diagnostics Corp. (East Walpole, US). The FDA issued a Cleared decision on January 14, 1987 after a review of 9 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

FDA 510(k) Submission Details - K870036

510(k) Number K870036 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 05, 1987
Decision Date January 14, 1987
Days to Decision 9 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
79d faster than avg
Panel avg: 88d · This submission: 9d
Pathway characteristics
Predicate-based equivalence.

JJS Device Classification - Class 1, General Controls

Product Code JJS Controls For Blood-gases, (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 - JJS Controls For Blood-gases, (assayed And Unassayed)

All 50
Devices cleared under the same product code (JJS) and FDA review panel - the closest regulatory comparables to K870036.
QUALICHECK 2
K894110 · Radiometer America, Inc. · Aug 1989
MULTI-FUNCTION BLOOD GAS CONTROL
K874408 · Bionostics, Inc. · Dec 1987
AQUEOUS BLOOD GAS/ELECTROLYTE CONTR LEV I,II & III
K872196 · American Dade · Jul 1987
MARQUEST QC-IV TONOMETER
K855024 · Marquest Medical Products, Inc. · Apr 1986
MULTI FUNCTION BLOOD GAS CONTROL
K851911 · Bionostics, Inc. · May 1985
BLOOD GAS CONTROL, LEVEL I(ACIDOSIS
K841783 · Bionostics, Inc. · Jun 1984