R.E. Brown Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
R.E. Brown Co., Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
R.E. Brown Co., Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1978 to 1978.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - R.E. Brown Co., Inc.
10 devices
Cleared
Dec 21, 1978
PACING LEAD MODEL BUS 860, BUS 890
Cardiovascular
92d
Cleared
Dec 08, 1978
PACING LEAD MODELS SA, 350, SAM 500
Cardiovascular
79d
Cleared
Dec 08, 1978
PACING LEAD MODELS, MDM 1060, MDM 1090
Cardiovascular
79d
Cleared
Dec 08, 1978
PACING LEAD MODELS, MAM 1260 MAM 1290
Cardiovascular
79d
Cleared
Dec 08, 1978
PACING LEAD ADAPTER MODEL ACS 16
Cardiovascular
79d
Cleared
Dec 08, 1978
PACING MODELS MUM 860, MUM 890
Cardiovascular
79d
Cleared
Dec 08, 1978
PACING LEAD MODEL MVM 860, MVM 890
Cardiovascular
79d
Cleared
Dec 08, 1978
PACING LEAD ADAPTER, ACV 14, ACV 23
Cardiovascular
79d
Cleared
Dec 08, 1978
PACING LEAD ADAPTER MODEL ADB 21
Cardiovascular
79d
Cleared
Jul 27, 1978
STILITH CARDIAC PACEMAKERS-M. 60 & 120
Cardiovascular
76d