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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
510(k) clearance decisions for Hoffrel Instruments, Inc., by decision year
YearClearances
19781
19791
19801
19833
19842
19852
19861
19871
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K870850MOD 482JOPSubstantially Equivalent
K860235MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCERITXSubstantially Equivalent
K850165MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417JOPSubstantially Equivalent
K844916MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLERIYOSubstantially Equivalent
K834277MOD 427IYOSubstantially Equivalent
K834276MOD 456IYOSubstantially Equivalent
K837282MODEL VPS VASCULAR PROFILE SYSTEMSubstantially Equivalent
K837229TRANSDUCER MODELS 450, 451, 452, 453, 454Substantially Equivalent
K837142TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEMSubstantially Equivalent
K800364ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202DKXSubstantially Equivalent
K790396ULTRASONIC DIAGNOSTIC SYSTEMIYOSubstantially Equivalent
K780651ULTRASONIC DIAGNOSTIC TRANSDUCERITXSubstantially 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

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Data as of , FDA export datePage updated Source: openFDA, public domain