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

ERG 550 ERGOMETER BICYCLE

K Number: K854491 · Decision Jun 16, 1986
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
21
Review Days
216

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Basic Information

Device Name
ERG 550 ERGOMETER BICYCLE
K Number
K854491
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Robert Bosch Corp.
Date Received
November 12, 1985
Decision Date
June 16, 1986
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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Other Clearances by Robert Bosch Corp.

K Number Device Name
K854493 ERG 555 COUCH ERGOMETER
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
K850186 POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &
Search all 21 clearances from Robert Bosch Corp. →