Company · US

Phoenix Glove Co.

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1983. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
FMC	Patient Examination Glove	2
DRX	Electrode, Electrocardiograph	1
FJZ	Declotting Tray, Kit (Including Contents)	1
FRG	Wrap, Sterilization	1
KKX	Drape, Surgical, Antimicrobial	1

Decided	510(k)	Device and applicant	Code
Mar 17, 1983	K830660	STERILE SURGICAL DRAPES Phoenix Glove Co.	KKX
Jun 23, 1982	K821044	PATIENT PREP KITS/TRAYS-STERILE Phoenix Glove Co.	FRG
Jun 21, 1982	K821666	STERILE SURGICAL DRAPES Phoenix Glove Co.	FJZ
May 21, 1982	K821043	STERILE PATIENT EXAM. GLOVES Phoenix Glove Co.	FMC
Sep 9, 1980	K801846	ELECTROCARDIOGRAPH ELECTRODE Phoenix Glove Co.	DRX
Dec 7, 1978	K781820	GLOVES, VINYL EXAMINATION Phoenix Glove Co.	FMC

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.