FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VACOMED 4

K Number: K842802 · Decision Aug 1, 1984
Classifications
1
FEI Numbers
759
Registration Numbers
759
Same Product Code
99
Applicant Total
21
Review Days
15

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Basic Information

Device Name
VACOMED 4
K Number
K842802
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5660
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Robert Bosch Corp.
Date Received
July 17, 1984
Decision Date
August 1, 1984
Product Code
ISA
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
ISA Massager, Therapeutic, Electric

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Other Clearances by Robert Bosch Corp.

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
K851937 SONOMED 4
K850188 BOSCH IN THE EAR HEARING AID SUPERSTAR
Search all 21 clearances from Robert Bosch Corp. →