Rastronics USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rastronics USA, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Rastronics USA, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mountainside, US.
Historical record: 5 cleared submissions from 1985 to 1990. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Rastronics USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rastronics USA, Inc.
5 devices
Cleared
Oct 05, 1990
RASTRONICS CCI 8
Ear, Nose, Throat
140d
Cleared
Sep 12, 1990
RASTRONICS CCI 10/3 HEARING AID ANALYSIS
Ear, Nose, Throat
114d
Cleared
Aug 09, 1990
RASTRONICS PORTAREM 20
Dental
79d
Cleared
Jun 21, 1989
HANDTYMP SCREENER MODEL 2000 + 2002 REMOTE TRANS.
Ear, Nose, Throat
120d
Cleared
Sep 27, 1985
FREQUENCY RESPONSE ANALYZER COMPUTER SYS CCI-10
Ear, Nose, Throat
59d