510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K970533Substantially Equivalent

Model 1100 Cold Therapy Device

Smith & Nephew, Inc., Carlsbad CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970533 is the FDA 510(k) clearance record for MODEL 1100 COLD THERAPY DEVICE, a class II device, cleared for Smith & Nephew, Inc. on under FDA product code ILO (Pack, Hot Or Cold, Water Circulating). FDA records list 572 510(k) clearances for Smith & Nephew, Inc., from to . As of , FDA records show no recalls naming K970533.

Clearance record

Decision date
Received
(62 days to decision)
Product code
ILO Pack, Hot Or Cold, Water Circulating
Regulation
21 CFR 890.5720
Device class
Class II
Review panel
Physical Medicine
Applicant
Smith & Nephew, Inc. 2777 Loker Ave., W., Carlsbad CA
510(k) summary
Summary
Third party review
No

Clearances, product code ILO

Trailing 12 months

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

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