Spectramed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spectramed, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Spectramed, Inc. has 13 FDA 510(k) cleared medical devices. Based in Findley, US.
Historical record: 13 cleared submissions from 1987 to 1990. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Spectramed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spectramed, Inc.
13 devices
Cleared
Jan 19, 1990
AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED
Obstetrics & Gynecology
87d
Cleared
Nov 06, 1989
CCO SYSTEM MODEL SP1467,SP5567,SP6267
Cardiovascular
199d
Cleared
Oct 24, 1989
MODEL DT-BAL, BALANCE SAVER
Obstetrics & Gynecology
56d
Cleared
Aug 15, 1989
MODEL DT-IUPC2 TRANSDUCER TIPPED DUAL LUMEN IUP
Obstetrics & Gynecology
32d
Cleared
Feb 01, 1989
AMNICATH(TM) MODEL DT-IUPC TRANS. TIPPED INTRAU.
Obstetrics & Gynecology
274d
Cleared
Jan 25, 1989
SAFE-DRAW(TM) BLOOD SAMPLING RESERVOIR & ACCESS.
Cardiovascular
36d
Cleared
Sep 28, 1988
MODELS SP5825/SP5835/SP5845/SP5855 PERCU. SHEATH
Cardiovascular
152d
Cleared
May 25, 1988
HEPARIN COATED LUMINAL PACING CATHETER
Cardiovascular
147d
Cleared
Mar 22, 1988
MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE
General Hospital
27d
Cleared
Jan 12, 1988
SPECTRAMED DISPOSABLE TRANSDUCER (DT-XXO) & ACCESS
Cardiovascular
154d
Cleared
Sep 16, 1987
CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS
Cardiovascular
147d
Cleared
Apr 20, 1987
SPECTRAMED MODEL SP1455 HEMOPRO2 SYSTEM
Cardiovascular
111d
Cleared
Mar 06, 1987
V-PACE(TM) TRANSLUMINAL VENTRICULAR/ MODEL SP5540
Cardiovascular
112d