Medical Device Manufacturer · US , Mchenry , IL

Hoffrel Instruments, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1978

Total

Cleared

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

1-12 of 12

Cleared Sep 08, 1987

MOD 482

K870850 · JOP

Cardiovascular · 189d

Cleared May 15, 1986

MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCER

K860235 · ITX

Radiology · 113d

Cleared Oct 23, 1985

MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417

K850165 · JOP

Cardiovascular · 280d

Cleared Apr 22, 1985

MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLER

MODEL VPS VASCULAR PROFILE SYSTEM

K837282

Radiology · 42d

Cleared Apr 15, 1983

TRANSDUCER MODELS 450, 451, 452, 453, 454

K837229

Radiology · 45d

Cleared Mar 23, 1983

TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM

K837142

Radiology · 79d

Cleared Mar 12, 1980

ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202

K800364 · DKX

Toxicology · 21d

Cleared Mar 21, 1979

ULTRASONIC DIAGNOSTIC SYSTEM

K790396 · IYO

Radiology · 23d

Cleared May 09, 1978

ULTRASONIC DIAGNOSTIC TRANSDUCER

K780651 · ITX

Radiology · 20d

Hoffrel Instruments, Inc. - FDA 510(k) Cleared Devices

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