FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

TELEPHONE RECEIVERS R101 R111

K Number: K840032 · Decision Oct 26, 1984
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
292
Applicant Total
5
Review Days
295

Basic Information

Device Name
TELEPHONE RECEIVERS R101 R111
K Number
K840032
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2920
Medical Specialty
Cardiovascular
Decision
Unknown
Applicant
BIOMETRIC PRODUCTS, INC.
Date Received
January 5, 1984
Decision Date
October 26, 1984
Product Code
DXH
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
DXH Transmitters And Receivers, Electrocardiograph, Telephone

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