510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802399Substantially Equivalent

Model 2500 Pneumatic Percussor

Medical Equipment Development Co., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802399 is the FDA 510(k) clearance record for MODEL 2500 PNEUMATIC PERCUSSOR, a class II device, cleared for Medical Equipment Development Co., Inc. on under FDA product code BYI (Percussor, Powered-Electric). FDA records list 7 510(k) clearances for Medical Equipment Development Co., Inc., from to . As of , FDA records show no recalls naming K802399.

Clearance record

Decision date
Received
(21 days to decision)
Product code
BYI Percussor, Powered-Electric
Regulation
21 CFR 868.5665
Device class
Class II
Review panel
Anesthesiology
Applicant
Medical Equipment Development Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BYI

Trailing 12 months
1 clearance under product code BYI in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BYI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260