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

MONITOR, HEARTWATCH HEART RATE

K Number: K770038 · Decision Jan 14, 1977
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
172
Review Days
4

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Basic Information

Device Name
MONITOR, HEARTWATCH HEART RATE
K Number
K770038
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Respironics, Inc.
Date Received
January 10, 1977
Decision Date
January 14, 1977
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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