Hoffrel Instruments, Inc.
Mchenry, IL, US
Hoffrel Instruments, Inc. appears in FDA device records in Mchenry, IL. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Hoffrel Instruments, Inc. between 1978 and 1987. The busiest year on record is 1983, with 3. The most recent is 1987, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1979 | 1 |
| 1980 | 1 |
| 1983 | 3 |
| 1984 | 2 |
| 1985 | 2 |
| 1986 | 1 |
| 1987 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K870850 | MOD 482 | JOP | Substantially Equivalent | |
| K860235 | MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCER | ITX | Substantially Equivalent | |
| K850165 | MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417 | JOP | Substantially Equivalent | |
| K844916 | MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLER | IYO | Substantially Equivalent | |
| K834277 | MOD 427 | IYO | Substantially Equivalent | |
| K834276 | MOD 456 | IYO | Substantially Equivalent | |
| K837282 | MODEL VPS VASCULAR PROFILE SYSTEM | Substantially Equivalent | ||
| K837229 | TRANSDUCER MODELS 450, 451, 452, 453, 454 | Substantially Equivalent | ||
| K837142 | TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM | Substantially Equivalent | ||
| K800364 | ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202 | DKX | Substantially Equivalent | |
| K790396 | ULTRASONIC DIAGNOSTIC SYSTEM | IYO | Substantially Equivalent | |
| K780651 | ULTRASONIC DIAGNOSTIC TRANSDUCER | ITX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
