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
K990233Substantially Equivalent

St-302 Infrarex

Skylark Device Co., Ltd., Taipei, TW / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K990233 is the FDA 510(k) clearance record for ST-302 INFRAREX, a class II device, cleared for Skylark Device Co., Ltd. on under FDA product code ILY (Lamp, Infrared, Therapeutic Heating). FDA records list 20 510(k) clearances for Skylark Device Co., Ltd., from to . As of , FDA records show no recalls naming K990233.

Clearance record

Decision date
Received
(275 days to decision)
Product code
ILY Lamp, Infrared, Therapeutic Heating
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Skylark Device Co., Ltd. 12fl., # 34, Sec. 3, Taipei, TW
510(k) summary
Statement
Third party review
No

Clearances, product code ILY

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