meddevicedb.com FDA Device Reference

Review Panel

Cardiovascular FDA 510(k) Clearances & Devices

Cleared Devices
19,212
Product Codes (page)
8
Latest Decision
1976-07-20

Clearances · page 193 of 193

K-Number Trade Name Applicant / Manufacturer Product Code Class Decision Date
K760136 CATHETER, THORACIC DRAIN Sherwood Medical Industries DWS Class I 1976-07-20
K760090 GRAFT, COOLEY GUIDELINE, STERILE Meadox Medicals, Div. Boston Scientific Corp. DSY Class II 1976-07-20
K760013 PACER SYSTEMS ANALYZER (CORDIS) Cordis Corp. DTC Class II 1976-07-20
K760091 GRAFT, MICROVEL GUIDELINE, STERILE Meadox Medicals, Div. Boston Scientific Corp. DSY Class II 1976-07-20
K760087 TAPE, VASCULAR, 1/4 DACRON Meadox Medicals, Div. Boston Scientific Corp. DWS Class I 1976-07-20
K760120 PULSE CARDULE (MODEL 1859/1860 ECG) Spacelabs, Inc. DRT Class II 1976-07-20
K760130 PROSTHESIS, VASCULAR BIFURCATED Usci, Div. C.R. Bard, Inc. DSY Class II 1976-07-20
K760192 COMPUTER, THERMODILUTION CARDIAC (9520) Edwards Laboratories DXG Class II 1976-07-19
K760160 MONITOR, PATIENT (MODEL 78333A) Hewlett-Packard Co. DRT Class II 1976-07-19
K760157 SPHYGMOMANOMETER Eyvirco DXQ Class II 1976-07-19
K760150 MONITOR, PATIENT (MODEL 78331A) Hewlett-Packard Co. DPS Class II 1976-07-19
K760152 FILTER (7220&7221 MOBIN-UDDIN VENA CAVA) Edwards Laboratories DTK Class II 1976-07-19

19,212 clearances in the Cardiovascular panel. Data: openFDA.