Cleared Traditional

K865051 - GRASEBY PCAS MODEL NO. 0124-0701

K865051 is an FDA 510(k) clearance for GRASEBY PCAS MODEL NO. 0124-0701, manufactured by Panamedix, Inc.. The device is a Class 2 General Hospital device with product code FRN cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K865051 · Panamedix, Inc. · General Hospital
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Feb 1987
Decision
48d
Days
Class 2
Risk

K865051 is an FDA 510(k) clearance for the GRASEBY PCAS MODEL NO. 0124-0701, PVS DYTINHR PUMP. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Panamedix, Inc. (Costa Mesa, US). The FDA issued a Cleared decision on February 10, 1987 after a review of 48 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 Panamedix, Inc. devices

FDA 510(k) Submission Details - K865051

510(k) Number K865051 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 24, 1986
Decision Date February 10, 1987
Days to Decision 48 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 129d · This submission: 48d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRN Device Classification - Class 2, Special Controls

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 460
Devices cleared under the same product code (FRN) and FDA review panel - the closest regulatory comparables to K865051.
HOMEPRO II VOLUMETRIC INFUSION PUMP
K870444 · American Edwards Laboratories · Apr 1987
MEDTRAC VP VOLUMETRIC INFUSION PUMP
K864997 · American Edwards Laboratories · Feb 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
I.V. SET WITH DUAL-CHANNEL CASSETTE
K865060 · Abbott Laboratories · Feb 1987