510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K964523Substantially Equivalent

Recover Infant Heel Warmer (5100)

Florida Medical Industries, Inc., Tarpon Springs FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K964523 is the FDA 510(k) clearance record for RECOVER INFANT HEEL WARMER (5100), a class I device, cleared for Florida Medical Industries, Inc. on under FDA product code MPO (Infant Heel Warmer (Chemical Heat Pack)). FDA records list 2 510(k) clearances for Florida Medical Industries, Inc., from to . As of , FDA records show 4 recalls naming K964523.

Clearance record

Decision date
Received
(90 days to decision)
Product code
MPO Infant Heel Warmer (Chemical Heat Pack)
Regulation
21 CFR 890.5710
Device class
Class I
Review panel
Physical Medicine
Applicant
Florida Medical Industries, Inc. 40178 u.s. 19 N., Tarpon Springs FL
510(k) summary
Summary
Third party review
No

Clearances, product code MPO

Trailing 12 months

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

FDA records show no clearances under product code MPO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MPO, 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