Cleared Traditional

K900104 - TCPM II TOURNIQUET CUFF PRESSURE MONITOR

K900104 is the FDA 510(k) clearance for TCPM II TOURNIQUET CUFF PRESSURE MONITOR by Electromedics, Inc.. It is a Class 1 General & Plastic Surgery device (product code KCY) cleared through the Traditional 510(k) pathway after a 65-day FDA review.

K900104 · Electromedics, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1990
Decision
65d
Days
Class 1
Risk

K900104 is an FDA 510(k) clearance for the TCPM II TOURNIQUET CUFF PRESSURE MONITOR. Classified as Tourniquet, Pneumatic (product code KCY), Class I - General Controls.

Submitted by Electromedics, Inc. (Englewood, US). The FDA issued a Cleared decision on March 15, 1990 after a review of 65 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.5910 - the FDA general and plastic surgery 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 Electromedics, Inc. devices

Submission Details

510(k) Number K900104 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 09, 1990
Decision Date March 15, 1990
Days to Decision 65 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 115d · This submission: 65d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KCY Tourniquet, Pneumatic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.5910
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 - KCY Tourniquet, Pneumatic

All 8
Devices cleared under the same product code (KCY) and FDA review panel - the closest regulatory comparables to K900104.
EXPRESSAIRE TORUNIQUET SYSTEM
K955552 · Smith & Nephew Richards, Inc. · Jan 1996
DEROYAL INDUSTRIES, INC. PNEUMATIC TOURNIQUET CUFF
K953953 · Deroyal Industries, Inc. · Sep 1995
ARTHREX TOURNIQUET FOR LEG HOLDER
K933994 · Arthrex, Inc. · Mar 1994
PRESSURE SENTRY TOURNIQUET
K840206 · Richards Medical Co., Inc. · Apr 1984
TEST PRESSURE GAUGE #6675-32
K791759 · Depuy, Inc. · Oct 1979