Cleared Traditional

K864997 - MEDTRAC VP VOLUMETRIC INFUSION PUMP

K864997 is the FDA 510(k) clearance for MEDTRAC VP VOLUMETRIC INFUSION PUMP by American Edwards Laboratories. It is a Class 2 General Hospital device (product code FRN) cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K864997 · American Edwards Laboratories · General Hospital
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Feb 1987
Decision
67d
Days
Class 2
Risk

K864997 is an FDA 510(k) clearance for the MEDTRAC VP VOLUMETRIC INFUSION PUMP. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by American Edwards Laboratories (Santa Ana, US). The FDA issued a Cleared decision on February 27, 1987 after a review of 67 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - the FDA general hospital 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 American Edwards Laboratories devices

Submission Details

510(k) Number K864997 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 22, 1986
Decision Date February 27, 1987
Days to Decision 67 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 129d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FRN Pump, Infusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
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 Hospital devices follow this clearance model.

Regulatory Peers - FRN Pump, Infusion

All 433
Devices cleared under the same product code (FRN) and FDA review panel - the closest regulatory comparables to K864997.
IMED(R) MODEL 960A VOLUMETRIC INFUSION PUMP
K870991 · Imed Corp. · Jun 1987
IMED(R) MODEL 965A VOLUMETRIC INFUSION PUMP
K870992 · Imed Corp. · Jun 1987
HOMEPRO II VOLUMETRIC INFUSION PUMP
K870444 · American Edwards Laboratories · Apr 1987
IVAC(R) STAR-FLOW(TM) VOLUMETRIC PUMP - MODEL 580
K864809 · Y · Feb 1987
ABBOTT LIFECARE (R) 5000, PUMP SYSTEM
K865058 · Abbott Laboratories · Feb 1987
I.V. SET W/SINGLE-CHANNEL CASSETTE
K865059 · Abbott Laboratories · Feb 1987