Cleared Traditional

K843274 - MODULAR VOLUMETRIC INFUSION PUMP SYS

K843274 is the FDA 510(k) clearance for MODULAR VOLUMETRIC INFUSION PUMP SYS by American Edwards Laboratories. It is a Class 2 General Hospital device (product code FRN) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K843274 · American Edwards Laboratories · General Hospital
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Oct 1984
Decision
60d
Days
Class 2
Risk

K843274 is an FDA 510(k) clearance for the MODULAR VOLUMETRIC INFUSION PUMP SYS. 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 October 19, 1984 after a review of 60 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 K843274 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 1984
Decision Date October 19, 1984
Days to Decision 60 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
69d faster than avg
Panel avg: 129d · This submission: 60d
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 K843274.
INTERMEDICS/GRASEBY DYNAMICS MS 36
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K842027 · Y · Jul 1984
ACCUPRO VOLUMETRIC INFUSION PUMP W/RS232
K841922 · American Edwards Laboratories · Jul 1984