FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417

K Number: K850165 · Decision Oct 23, 1985
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
12
Review Days
280

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Basic Information

Device Name
MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417
K Number
K850165
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Hoffrel Instruments, Inc.
Date Received
January 16, 1985
Decision Date
October 23, 1985
Product Code
JOP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOP Transducer, Ultrasonic

Similar 510(k) Clearances

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Other Clearances by Hoffrel Instruments, Inc.

K Number Device Name
K870850 MOD 482
K860235 MOD 426, MEDICAL ULTRASONIC DIAGNOSTC TRANSDUCER
K844916 MODEL 518 & 519 ULTRASONOSCOPE W/DOPPLER
K834276 MOD 456
K834277 MOD 427
K837282 MODEL VPS VASCULAR PROFILE SYSTEM
K837229 TRANSDUCER MODELS 450, 451, 452, 453, 454
K837142 TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM
K800364 ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202
K790396 ULTRASONIC DIAGNOSTIC SYSTEM
Search all 12 clearances from Hoffrel Instruments, Inc. →