Bio Mega Diagnostic, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bio Mega Diagnostic, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Bio Mega Diagnostic, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1976 to 1987. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bio Mega Diagnostic, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bio Mega Diagnostic, Inc.
5 devices
Cleared
Feb 04, 1987
BIO-MEGA DIAGNOSTIC COATED TUBE IRMA TSH
Chemistry
68d
Cleared
Sep 21, 1982
BIOMEGA MODEL 59W
Cardiovascular
39d
Cleared
Jan 22, 1982
MOD. 587 BLOOD PRESSURE & PULSE MONITOR
Cardiovascular
31d
Cleared
Aug 27, 1980
BIOMEGA #423-B BLOOD PRESSURE & PULSE CK
Cardiovascular
15d
Cleared
Nov 09, 1976
BLOOD PRESSURE & PULSE CHECKER
Cardiovascular
11d