Cleared Traditional

K862973 - STOCKERT-SHILEY CAPS TIMER MODULE

K862973 is an FDA 510(k) clearance for STOCKERT-SHILEY CAPS TIMER MODULE, manufactured by Shiley, Inc.. The device is a Class 2 Cardiovascular device with product code DTQ cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K862973 · Shiley, Inc. · Cardiovascular device
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Oct 1986
Decision
56d
Days
Class 2
Risk

K862973 is an FDA 510(k) clearance for the STOCKERT-SHILEY CAPS TIMER MODULE. Classified as Console, Heart-lung Machine, Cardiopulmonary Bypass (product code DTQ), Class II - Special Controls.

Submitted by Shiley, Inc. (Irvine, US). The FDA issued a Cleared decision on October 1, 1986 after a review of 56 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4220 - 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 Shiley, Inc. devices

FDA 510(k) Submission Details - K862973

510(k) Number K862973 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 06, 1986
Decision Date October 01, 1986
Days to Decision 56 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 125d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DTQ Device Classification - Class 2, Special Controls

Product Code DTQ Console, Heart-lung Machine, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4220
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 - DTQ Console, Heart-lung Machine, Cardiopulmonary Bypass

All 26
Devices cleared under the same product code (DTQ) and FDA review panel - the closest regulatory comparables to K862973.
ONGUARD 1000, CATALOG #043611-000 & 043611-001
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STOCKERT-SHILEY CAPS BATTERY MODULE
K863960 · Shiley, Inc. · Dec 1986
STOCKERT-SHILEY CAPS HLM INTERFACE
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SARNS PORTABLE POWER MODULE
K861388 · 3M Health Care, Sarns · Jun 1986
COBE EMERGENCY POWER SOURCE 43610-000
K842138 · Cobe Laboratories, Inc. · Aug 1984
GAMBRO PUMP CONSOLE CSL
K822068 · Gambro, Inc. · Aug 1982