Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K960999Substantially Equivalent

Isolation Gown

Copioumed Intl., Inc., Taipei, Taaaaiwan R.O.C., TW / Traditional, Substantially Equivalent

K960999 is the FDA 510(k) clearance record for ISOLATION GOWN, a class II device, cleared for Copioumed Intl., Inc. on under FDA product code FYC (Gown, Isolation, Surgical). FDA records list 8 510(k) clearances for Copioumed Intl., Inc., from to . As of , FDA records show no recalls naming K960999.

Clearance record

Decision date
Received
(293 days to decision)
Product code
FYC Gown, Isolation, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Copioumed Intl., Inc. 6f-1 # 169-12, Sec. 2, Taipei, Taaaaiwan R.O.C., TW
510(k) summary
Statement
Third party review
No

Clearances, product code FYC

Trailing 12 months

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

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