Hoffrel Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hoffrel Instruments, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Hoffrel Instruments, Inc. has 12 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1978 to 1987.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hoffrel Instruments, Inc.
12 devices
Cleared
Sep 08, 1987
MOD 482
Cardiovascular
189d
Cleared
May 15, 1986
MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCER
Radiology
113d
Cleared
Oct 23, 1985
MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417
Cardiovascular
280d
Cleared
Apr 22, 1985
MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLER
Radiology
125d
Cleared
Feb 17, 1984
MOD 456
Radiology
109d
Cleared
Feb 17, 1984
MOD 427
Radiology
109d
Cleared
Apr 26, 1983
MODEL VPS VASCULAR PROFILE SYSTEM
Radiology
42d
Cleared
Apr 15, 1983
TRANSDUCER MODELS 450, 451, 452, 453, 454
Radiology
45d
Cleared
Mar 23, 1983
TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM
Radiology
79d
Cleared
Mar 12, 1980
ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202
Toxicology
21d
Cleared
Mar 21, 1979
ULTRASONIC DIAGNOSTIC SYSTEM
Radiology
23d
Cleared
May 09, 1978
ULTRASONIC DIAGNOSTIC TRANSDUCER
Radiology
20d