Cleared Traditional

K860556 - SERIES 7050 CAPNOGRAPH

K860556 is the FDA 510(k) clearance for SERIES 7050 CAPNOGRAPH by Marquette Electronics, Inc.. It is a Class 2 Anesthesiology device (product code CCK) cleared through the Traditional 510(k) pathway after a 7-day FDA review.

K860556 · Marquette Electronics, Inc. · Anesthesiology device
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Feb 1986
Decision
7d
Days
Class 2
Risk

K860556 is an FDA 510(k) clearance for the SERIES 7050 CAPNOGRAPH. Classified as Analyzer, Gas, Carbon-dioxide, Gaseous-phase (product code CCK), Class II - Special Controls.

Submitted by Marquette Electronics, Inc. (Milwaukee, US). The FDA issued a Cleared decision on February 21, 1986 after a review of 7 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1400 - the FDA anesthesiology and respiratory 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 Marquette Electronics, Inc. devices

Submission Details

510(k) Number K860556 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 14, 1986
Decision Date February 21, 1986
Days to Decision 7 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
133d faster than avg
Panel avg: 140d · This submission: 7d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CCK Analyzer, Gas, Carbon-dioxide, Gaseous-phase
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1400
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Anesthesiology devices follow this clearance model.

Regulatory Peers - CCK Analyzer, Gas, Carbon-dioxide, Gaseous-phase

All 147
Devices cleared under the same product code (CCK) and FDA review panel - the closest regulatory comparables to K860556.
MODULAR MASS SPECTROMETER (M.S.)
K862605 · The Perkin-Elmer Corp. · Aug 1986
DYNEX CO2/2000, CO2 ANALYZER
K862543 · Analytical Products, Inc. · Jul 1986
PB 254 IR - SPECTROMETER
K861213 · Datex Division Instrumentarium Corp. · Apr 1986
CAPNOMED
K851658 · Draeger Medical, Inc. · May 1985
SERIES 7000 END TIDAL CO2 MONITORING SYSTEM
K851001 · Marquette Electronics, Inc. · May 1985
TRI-MED MODEL 112 MOISTURE TRAP
K850745 · Tri-Med, Inc. · Apr 1985