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

SONOPULS 463, ULTRASOUND THERAPY EQUIPMENT

K Number: K872393 · Decision Jul 23, 1987
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
88
Applicant Total
44
Review Days
41

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Basic Information

Device Name
SONOPULS 463, ULTRASOUND THERAPY EQUIPMENT
K Number
K872393
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5300
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Henley Intl.
Date Received
June 12, 1987
Decision Date
July 23, 1987
Product Code
IMI
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

Similar 510(k) Clearances

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Other Clearances by Henley Intl.

K Number Device Name
K943449 NEUROLOGICAL DIAGNOSTIC DEVICES
K926279 UPPER BODY EXERCISER
K926278 STAIR CLIMBER
K926287 EXERCISE BICYCLE
K926314 HYDRA FITNESS MODEL 311 TOTAL POWER
K926313 COMPUTERIZED TESTING AND EXERCISE SYSTEMS
K915864 MONOTRODE CUTANEOUS ELECTRODE
K922036 SONOPULS 591
K926316 TRUE-TRAC, STRATUS
K920983 SONOPULS 590
Search all 44 clearances from Henley Intl. →