Cleared Traditional

K802399 - MODEL 2500 PNEUMATIC PERCUSSOR

K802399 is an FDA 510(k) clearance for MODEL 2500 PNEUMATIC PERCUSSOR, manufactured by Medical Equipment Development Co., Inc.. The device is a Class 2 Anesthesiology device with product code BYI cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K802399 · Medical Equipment Development Co., Inc. · Anesthesiology device
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Oct 1980
Decision
21d
Days
Class 2
Risk

K802399 is an FDA 510(k) clearance for the MODEL 2500 PNEUMATIC PERCUSSOR. Classified as Percussor, Powered-electric (product code BYI), Class II - Special Controls.

Submitted by Medical Equipment Development Co., Inc. (Mchenry, US). The FDA issued a Cleared decision on October 23, 1980 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5665 - the FDA anesthesiology and respiratory 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 Medical Equipment Development Co., Inc. devices

FDA 510(k) Submission Details - K802399

510(k) Number K802399 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 02, 1980
Decision Date October 23, 1980
Days to Decision 21 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
119d faster than avg
Panel avg: 140d · This submission: 21d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BYI Device Classification - Class 2, Special Controls

Product Code BYI Percussor, Powered-electric
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5665
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - BYI Percussor, Powered-electric

All 35
Devices cleared under the same product code (BYI) and FDA review panel - the closest regulatory comparables to K802399.
INFANT PERCUSSOR #5534
K812803 · Hudson Oxygen Therapy Sales Co. · Dec 1981
PERCUSSOR
K812166 · Dhd Medical Products Div. Diemolding Corp. · Aug 1981
HAND PERCUSSOR CUP #65210
K802646 · B & F Medical Products, Inc. · Nov 1980
5300 PERCUSSOR
K790675 · Hudson Oxygen Therapy Sales Co. · Apr 1979
ARGYLE PEOCUSSOR SYSTEM
K771876 · Sherwood Medical Industries · Oct 1977