Burditt & Calkins-Siemens-Elema is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Burditt & Calkins-Siemens-Elema - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Burditt & Calkins-Siemens-Elema has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1976 to 1984. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Burditt & Calkins-Siemens-Elema Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Burditt & Calkins-Siemens-Elema
10 devices
Cleared
Jan 30, 1984
PULSE GENERATOR MODEL 688
Cardiovascular
111d
Cleared
Jan 26, 1984
RAYDEN MEDICAL MINI PULSE VOLUME RECORD
Cardiovascular
133d
Cleared
May 27, 1983
SIEMENS-ELMA PULSE GENERATOR #718
Cardiovascular
114d
Cleared
Dec 30, 1982
MON-A-THERM MYOCARDIAL TEMP. SENSOR
Cardiovascular
44d
Cleared
Dec 28, 1982
AMEDA HAND BREAST PUMP
Obstetrics & Gynecology
22d
Cleared
Oct 04, 1982
COAXIAL BIPOLAR PACING ELECTRODE
Cardiovascular
68d
Cleared
Jul 26, 1982
INFORMED REMOTE FIELD UNIT MODEL IFM1000
Anesthesiology
47d
Cleared
Jan 23, 1981
ERECTAID
Gastroenterology & Urology
44d
Cleared
Nov 19, 1980
TERPERATUR SENSING DEVICE
General Hospital
29d
Cleared
Oct 22, 1976
LIBERATOR/STROLLER
Anesthesiology
16d