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

ECS 502

K Number: K840717 · Decision Aug 19, 1985
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
21
Review Days
549

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Basic Information

Device Name
ECS 502
K Number
K840717
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Robert Bosch Corp.
Date Received
February 17, 1984
Decision Date
August 19, 1985
Product Code
DRT
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
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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K853154 HV-4
K853271 HEARING AID ANALYSIS SYSTEM
K851485 DEFI 502
K851937 SONOMED 4
K850188 BOSCH IN THE EAR HEARING AID SUPERSTAR
K850186 POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &
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