Cunningham Woodland, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cunningham Woodland, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Cunningham Woodland, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1981 to 1983.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cunningham Woodland, Inc.
10 devices
Cleared
Mar 31, 1983
SUBCLAVIAN INSERTION KIT
General Hospital
121d
Cleared
Jan 22, 1982
PRE-PACK TENS
General & Plastic Surgery
60d
Cleared
Jan 05, 1982
NON-ABSORBENT TOWELS
General Hospital
20d
Cleared
Dec 29, 1981
VENOUS CANNULA TRAY
Cardiovascular
36d
Cleared
May 08, 1981
DRESSING TRAY MERCY HOSPITAL
General & Plastic Surgery
17d
Cleared
May 08, 1981
ONE STEP PREP KIT
General & Plastic Surgery
17d
Cleared
May 08, 1981
MAJOR DRESSING TRAY
General & Plastic Surgery
17d
Cleared
May 08, 1981
MINOR DRESSING TRAY
General & Plastic Surgery
17d
Cleared
May 01, 1981
SUTURE REMOVAL SET(DISPLSABLE)
General & Plastic Surgery
10d
Cleared
May 01, 1981
MIKA SKIN SCRUB TRAY PRE OPERATIVE W/GEL
General & Plastic Surgery
10d