Company · US

Hancock Laboratories, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1980. 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
DQO	Catheter, Intravascular, Diagnostic	1
DTI	Sizer, Heart-Valve, Prosthesis	1
DWS	Instruments, Surgical, Cardiovascular	1
KRH	Ring, Annuloplasty	1

Decided	510(k)	Device and applicant	Code
Sep 9, 1980	K801885	*HANCOCK OBTURATORS** Hancock Laboratories, Inc.	DTI
Apr 8, 1980	K800703	MODIFIED CATHETER PACKAGE Hancock Laboratories, Inc.	DQO
Feb 1, 1980	K800122	HANCOCK AORTIC PUNCH Hancock Laboratories, Inc.	DWS
Mar 26, 1979	K790534	MERSILENE SUTURES Hancock Laboratories, Inc.	KRH
May 26, 1978	K780568	DURAN FLEXIBLE RING Hancock Laboratories, Inc.

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