Cypress Medical Products, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cypress Medical Products, Ltd. - FDA 510(k) Cleared Devices
26
Total
19
Cleared
0
Denied
Cypress Medical Products, Ltd. has 19 FDA 510(k) cleared medical devices. Based in Mc Henry, US.
Historical record: 19 cleared submissions from 1989 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cypress Medical Products, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cypress Medical Products, Ltd.
26 devices
Cleared
Jul 12, 2002
CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL
Obstetrics & Gynecology
52d
Cleared
Aug 06, 2001
STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE
General Hospital
17d
Cleared
Jul 07, 1998
CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETER
Cardiovascular
335d
Cleared
May 28, 1998
ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
General Hospital
300d
Cleared
Feb 26, 1998
ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
General Hospital
205d
Cleared
Jul 05, 1995
CYPRESS MEDICAL PRODUCTS VINYL EXAMINATION GLOVE
General Hospital
55d
Cleared
Mar 31, 1995
CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE
General Hospital
67d
Cleared
Feb 27, 1995
CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY
Gastroenterology & Urology
48d
Cleared
Feb 27, 1995
CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY/WITH OUT CATHETER
Gastroenterology & Urology
47d
Cleared
Dec 08, 1994
CYPRESS MEDICAL PRODUCTS STETHOSCOPE
Cardiovascular
52d
Cleared
Nov 19, 1992
LACERATION REPAIR TRAY
General & Plastic Surgery
205d
Cleared
Oct 19, 1992
DRESSING CHANG & WOUND MANAGEMENT
General Hospital
264d