Cleared Traditional

K820739 - KEYMED KEY VAC SUCTION PUMP

K820739 is an FDA 510(k) clearance for KEYMED KEY VAC SUCTION PUMP, manufactured by Keymed, Inc.. The device is a Class 2 General & Plastic Surgery device with product code BTA cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K820739 · Keymed, Inc. · General & Plastic Surgery device
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May 1982
Decision
64d
Days
Class 2
Risk

K820739 is an FDA 510(k) clearance for the KEYMED KEY VAC SUCTION PUMP. Classified as Pump, Portable, Aspiration (manual Or Powered) (product code BTA), Class II - Special Controls.

Submitted by Keymed, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 21, 1982 after a review of 64 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4780 - 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 Keymed, Inc. devices

FDA 510(k) Submission Details - K820739

510(k) Number K820739 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 18, 1982
Decision Date May 21, 1982
Days to Decision 64 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 115d · This submission: 64d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTA Device Classification - Class 2, Special Controls

Product Code BTA Pump, Portable, Aspiration (manual Or Powered)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4780
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - BTA Pump, Portable, Aspiration (manual Or Powered)

All 106
Devices cleared under the same product code (BTA) and FDA review panel - the closest regulatory comparables to K820739.
EMERGENCY ASPIRATOR
K833785 · Vitalograph , Ltd. · Dec 1983
PSI SURGICAL ASPIRATOR
K832100 · Advanced Biosearch Assn. · Oct 1983
CONNECTING TUBES
K831007 · Medovations, Inc. · May 1983
IMPACT, MODELS 306/307
K820338 · Impact Instrumentation, Inc. · Mar 1982
GOMCO SUCTION PUMP CABINET CHANGE
K810490 · Allied Healthcare Products, Inc. · Mar 1981
SYSTEC 280 INTEGRATED SUCTION SYSTEM
K791349 · Stryker Corp. · Sep 1979