Company · US

Cooper Medical Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1984. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
FCG	Biopsy Needle	1
HHR	Laser, Surgical, Gynecologic	1
HQE	Instrument, Vitreous Aspiration And Cutting, Ac-Powered	1
LLF	Laser, Neurosurgical, Argon	1

Decided	510(k)	Device and applicant	Code
May 18, 1984	K840144	YAG LASER 8000 GASTROINTESTINAL BLEE Cooper Medical Corp.	FCG
Apr 18, 1984	K833387	ARGON LASER SURGICAL SYSTEM 770 Cooper Medical Corp.
Apr 17, 1984	K833497	COOPER MEDICAL MODEL 770 Cooper Medical Corp.	LLF
Jan 30, 1984	K832703	ARGON LASER SYS-MODEL 5000 Cooper Medical Corp.	HQE
Mar 5, 1982	K820261	MONITOR CO2 LASER SYSTEM Cooper Medical Corp.	HHR

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