Davis & Geck, Inc. - FDA 510(k) Cleared Devices
45
Total
42
Cleared
0
Denied
Davis & Geck, Inc. has 42 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 42 cleared submissions from 1981 to 1999.
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.
45 devices
Cleared
Apr 30, 1999
SILK SUTURE
General & Plastic Surgery
260d
Cleared
Jul 13, 1998
SURGILON, DERMALON, & OPHTHALON
General & Plastic Surgery
70d
Cleared
May 18, 1998
ARGYLE QUICK- PICC PERIPHERALLY INSERTED CENTRAL CATHETER- PICC TRAYS, ARGYLE...
General Hospital
208d
Cleared
May 18, 1998
DEXON RAPID (DEXON R)
General & Plastic Surgery
90d
Cleared
Mar 20, 1998
MONOJECTT BLUNTIP I.V. ACCESS CANNULA WITH VIAL ACCESS PIN DEVICE
General Hospital
72d
Cleared
Feb 27, 1998
KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS
Gastroenterology & Urology
171d
Cleared
Nov 05, 1997
ARGYLE AQUA-SEAL ALL PURPOSE AUTOTRANSFUSION CHEST DRAINAGE UNIT AND OPTIONAL...
Anesthesiology
240d
Cleared
Sep 03, 1997
ASPR-CARE CLOSED SYSTEM,DUAL SWIVEL PIECE T,SHEATHED SUCTION...
Anesthesiology
89d
Cleared
Aug 14, 1997
DEXON VIOLET
General & Plastic Surgery
36d
Cleared
Sep 16, 1996
POLYPROPYLENE MESH (VARIOUS SIZES)
General & Plastic Surgery
47d
Cleared
Mar 15, 1996
FLEXON TEMPORARY CARDIAC PACER LEAD
Cardiovascular
88d
Cleared
Feb 27, 1996
STAINLESS STEEL SUTURES, FLEXON STEEL SUTURES (STAINLESS)
General & Plastic Surgery
71d
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