Cleared Traditional

K831225 - GAS-STAT MONITORING SYSTEM

K831225 is an FDA 510(k) clearance for GAS-STAT MONITORING SYSTEM, manufactured by Cardiovascular Devices, Inc.. The device is a Class 2 Cardiovascular device with product code DRY cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K831225 · Cardiovascular Devices, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1983
Decision
42d
Days
Class 2
Risk

K831225 is an FDA 510(k) clearance for the GAS-STAT MONITORING SYSTEM. Classified as Monitor, Blood-gas, On-line, Cardiopulmonary Bypass (product code DRY), Class II - Special Controls.

Submitted by Cardiovascular Devices, Inc. (Walker, US). The FDA issued a Cleared decision on May 27, 1983 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4330 - the FDA cardiovascular device oversight 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 Cardiovascular Devices, Inc. devices

FDA 510(k) Submission Details - K831225

510(k) Number K831225 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 15, 1983
Decision Date May 27, 1983
Days to Decision 42 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
83d faster than avg
Panel avg: 125d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DRY Device Classification - Class 2, Special Controls

Product Code DRY Monitor, Blood-gas, On-line, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4330
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DRY Monitor, Blood-gas, On-line, Cardiopulmonary Bypass

All 33
Devices cleared under the same product code (DRY) and FDA review panel - the closest regulatory comparables to K831225.
STAT-SAT
K874839 · Gish Biomedical, Inc. · May 1988
HEMATOCRIT-SATURATION MONITOR HSM-100
K852124 · American Bentley · Sep 1985
COBE SATURATION CELL
K843709 · Cobe Laboratories, Inc. · Oct 1984
OXYGEN CONSUMPTION MONITOR #OCM-0100
K823359 · Bentley Laboratories, Inc. · Jan 1983
IN-LINE OXYGEN MONITORING SYSTEM
K821159 · G.D. Searle and Co. · May 1982