Hoffrel Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K870850 | MOD 482 | September 8, 1987 |
| K860235 | MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCER | May 15, 1986 |
| K850165 | MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 | October 23, 1985 |
| K844916 | MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLER | April 22, 1985 |
| K834277 | MOD 427 | February 17, 1984 |
| K834276 | MOD 456 | February 17, 1984 |
| K837282 | MODEL VPS VASCULAR PROFILE SYSTEM | April 26, 1983 |
| K837229 | TRANSDUCER MODELS 450, 451, 452, 453, 454 | April 15, 1983 |
| K837142 | TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM | March 23, 1983 |
| K800364 | ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202 | March 12, 1980 |
| K790396 | ULTRASONIC DIAGNOSTIC SYSTEM | March 21, 1979 |
| K780651 | ULTRASONIC DIAGNOSTIC TRANSDUCER | May 9, 1978 |