Cleared Traditional

K972962 - 3M CDI BLOOD PARAMETER MONITORING SYSTE...

K972962 is the FDA 510(k) clearance for 3M CDI BLOOD PARAMETER MONITORING SYSTE... by 3M Company. It is a Class 2 Cardiovascular device (product code DRY) cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K972962 · 3M Company · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1997
Decision
87d
Days
Class 2
Risk

K972962 is an FDA 510(k) clearance for the 3M CDI BLOOD PARAMETER MONITORING SYSTEM 500. Classified as Monitor, Blood-gas, On-line, Cardiopulmonary Bypass (product code DRY), Class II - Special Controls.

Submitted by 3M Company (Tustin, US). The FDA issued a Cleared decision on November 6, 1997 after a review of 87 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 3M Company devices

Submission Details

510(k) Number K972962 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 11, 1997
Decision Date November 06, 1997
Days to Decision 87 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
38d faster than avg
Panel avg: 125d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 20
Devices cleared under the same product code (DRY) and FDA review panel - the closest regulatory comparables to K972962.
CDI BLOOD PARAMETER MONITORING SYSTEM 500
K133658 · Terumo Cardiovascular Systems Corp. · Jul 2014
CDI BLOOD PARAMETER MONITORING SYSTEM 500
K123039 · Terumo Cardiovascular Systems Corp. · Nov 2012
BLOOD MONITORING UNIT, MODEL BMU 40
K090147 · Maquet Cardiopulmonary, AG · Apr 2009
CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO
K931968 · 3M Health Care, Ltd. · Nov 1993
CDI(TM) 300, 400 & 100, MODIFICATION
K915255 · 3M Company · Jan 1992
CDI(TM) H/S CUVETTE, MODIFICATION
K915265 · 3M Company · Jan 1992