Cleared Traditional

K936220 - DIDECO VACUUM PUMP

K936220 is an FDA 510(k) clearance for DIDECO VACUUM PUMP, manufactured by Dideco. The device is a Class 2 Anesthesiology device with product code CAC cleared through the Traditional 510(k) pathway after a 395-day FDA review.

K936220 · Dideco · Anesthesiology device
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Jan 1995
Decision
395d
Days
Class 2
Risk

K936220 is an FDA 510(k) clearance for the DIDECO VACUUM PUMP. Classified as Apparatus, Autotransfusion (product code CAC), Class II - Special Controls.

Submitted by Dideco (Mirandola ( Modena), IT). The FDA issued a Cleared decision on January 27, 1995 after a review of 395 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5830 - 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: Standard predicate-based submission. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Dideco devices

FDA 510(k) Submission Details - K936220

510(k) Number K936220 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 28, 1993
Decision Date January 27, 1995
Days to Decision 395 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
255d slower than avg
Panel avg: 140d · This submission: 395d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CAC Device Classification - Class 2, Special Controls

Product Code CAC Apparatus, Autotransfusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5830
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 - CAC Apparatus, Autotransfusion

All 166
Devices cleared under the same product code (CAC) and FDA review panel - the closest regulatory comparables to K936220.
BOEHRINGER AUTOVAC(R) 7900 SERIES
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K942791 · Sherwood Medical Co. · May 1995
DAVOL ATS
K931899 · Davol, Inc. · Nov 1994
PLEUR-EVAC CARDIOTOMY RESERVOIR # CR-9400 & 9400F
K926338 · Deknatel, Inc. · Jul 1994
AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S
K932093 · Boehringer Laboratories · Jul 1994