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

SONOMED 4

K Number: K851937 · Decision Jul 17, 1985
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
88
Applicant Total
21
Review Days
93

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Basic Information

Device Name
SONOMED 4
K Number
K851937
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5300
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Robert Bosch Corp.
Date Received
April 15, 1985
Decision Date
July 17, 1985
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

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K Number Device Name
K854493 ERG 555 COUCH ERGOMETER
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K854492 ERG 551 ERGOMETER, BICYCLE
K853541 SP 4
K853154 HV-4
K853271 HEARING AID ANALYSIS SYSTEM
K851485 DEFI 502
K840717 ECS 502
K850188 BOSCH IN THE EAR HEARING AID SUPERSTAR
K850186 POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &
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