Cleared Traditional

K801008 - MULTI-AD FLUID DISPENSING PUMP MP-3000 (FDA 510(k) Clearance)

Class I General Hospital device.

K801008 · Burron Medical Products, Inc. · General Hospital
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Jun 1980
Decision
35d
Days
Class 1
Risk

K801008 is an FDA 510(k) clearance for the MULTI-AD FLUID DISPENSING PUMP MP-3000. Classified as Dispenser, Liquid Medication (product code KYX), Class I - General Controls.

Submitted by Burron Medical Products, Inc. (Walker, US). The FDA issued a Cleared decision on June 2, 1980 after a review of 35 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6430 - 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 Burron Medical Products, Inc. devices

Submission Details

510(k) Number K801008 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 28, 1980
Decision Date June 02, 1980
Days to Decision 35 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
93d faster than avg
Panel avg: 128d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KYX Dispenser, Liquid Medication
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6430
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.