510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771824Substantially Equivalent

Medpro Flotation System

Medpro, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771824 is the FDA 510(k) clearance record for MEDPRO FLOTATION SYSTEM, a class I device, cleared for Medpro, Inc. on under FDA product code IKY (Mattress, Flotation Therapy, Non-Powered). FDA records list 4 510(k) clearances for Medpro, Inc., from to . As of , FDA records show no recalls naming K771824.

Clearance record

Decision date
Received
(22 days to decision)
Product code
IKY Mattress, Flotation Therapy, Non-Powered
Regulation
21 CFR 880.5150
Device class
Class I
Review panel
General Hospital
Applicant
Medpro, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IKY

Trailing 12 months

FDA records hold no clearances under product code IKY in the trailing twelve months.

FDA records show no clearances under product code IKY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IKY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260