510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K781539Substantially Equivalent

ISO-Care Kit

Nice-Pak Products, LLC, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781539 is the FDA 510(k) clearance record for ISO-CARE KIT, a class I device, cleared for Nice-Pak Products, Inc. on under FDA product code HMP (Pad, Eye). FDA records list 9 510(k) clearances for Nice-Pak Products, Inc., from to . As of , FDA records show no recalls naming K781539.

Clearance record

Decision date
Received
(56 days to decision)
Product code
HMP Pad, Eye
Regulation
21 CFR 878.4440
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Nice-Pak Products, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code HMP

Trailing 12 months

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

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