Cleared Traditional

K781271 - MONITOR, PO2, INTRAVASCULAR

K781271 is an FDA 510(k) clearance for MONITOR, manufactured by Roche Medical Electronics, Inc.. The device is a Class 2 Anesthesiology device with product code CCE cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K781271 · Roche Medical Electronics, Inc. · Anesthesiology device
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Oct 1978
Decision
80d
Days
Class 2
Risk

K781271 is an FDA 510(k) clearance for the MONITOR, PO2, INTRAVASCULAR. Classified as Analyzer, Gas, Oxygen, Partial Pressure, Blood-phase, Indwelling (product code CCE), Class II - Special Controls.

Submitted by Roche Medical Electronics, Inc. (Walker, US). The FDA issued a Cleared decision on October 12, 1978 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.1200 - 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 Roche Medical Electronics, Inc. devices

FDA 510(k) Submission Details - K781271

510(k) Number K781271 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 24, 1978
Decision Date October 12, 1978
Days to Decision 80 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 140d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CCE Device Classification - Class 2, Special Controls

Product Code CCE Analyzer, Gas, Oxygen, Partial Pressure, Blood-phase, Indwelling
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1200
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 - CCE Analyzer, Gas, Oxygen, Partial Pressure, Blood-phase, Indwelling

All 16
Devices cleared under the same product code (CCE) and FDA review panel - the closest regulatory comparables to K781271.
OXYGEN MONITOR NO. OM-100, OXYGEN PROBE NO. OP-100
K860106 · American Bentley · Feb 1986
OXYGEN MONITOR OM-100 & OXYGEN PROBE OP-100
K853786 · American Bentley · Oct 1985
VENOUS OXYGEN PROBE
K811071 · G.D. Searle and Co. · May 1981
CATHETER, PO2, INTRAVASUCLAR, CITADEL
K771116 · Sherwood Medical Industries · Sep 1977
MONITOR, CITADEL INTRAVASCULAR PO2
K760350 · Sherwood Medical Industries · Oct 1976