Berman, Pcp & Consultants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Berman, Pcp & Consultants, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Berman, Pcp & Consultants, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1977 to 1978. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Berman, Pcp & Consultants, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Berman, Pcp & Consultants, Inc.
7 devices
Cleared
Jan 05, 1978
SCALP VEIN SET
General Hospital
79d
Cleared
Sep 12, 1977
INFUSION SET TYPE S
General Hospital
84d
Cleared
Sep 12, 1977
INFUSION SET TYPE J
General Hospital
84d
Cleared
Sep 12, 1977
BLOOD COLLECTION SET TYPE H
General Hospital
84d
Cleared
Sep 12, 1977
BLOOD ADMINISTRATION TYPE R
General Hospital
84d
Cleared
Sep 12, 1977
SCALP VEIN SET
General Hospital
84d
Cleared
Sep 12, 1977
DISP. SYRINGES: 2,5 & L0 MI.
Microbiology
84d