Rozinn Electronics, Inc. is one of 13424 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rozinn Electronics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HOLTER PLUS
6
Total
6
Cleared
0
Denied
Rozinn Electronics, Inc. has 6 FDA 510(k) cleared medical devices. Based in Glendale, US.
Historical record: 6 cleared submissions from 1990 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Rozinn Electronics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Rozinn Electronics, Inc.
6 devices
Cleared
Sep 15, 2006
TELEPHONE ELECTROCARDIOGRAPH TRANSMITTER AND RECEIVER, TTM FOR WINDOWS +
Cardiovascular
81d
Cleared
Sep 22, 2004
HOLTER PLUS
Cardiovascular
9d
Cleared
Oct 24, 2002
CARDIO ID+(RZ153+)
Cardiovascular
84d
Cleared
Jul 24, 2002
ABP FOR WINDOWS
Cardiovascular
75d
Cleared
Apr 05, 2002
NETLINK/NETSCAN
Cardiovascular
73d
Cleared
Oct 22, 1990
ROZINN 151
Cardiovascular
89d