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

HR 100T

K Number: K831955 · Decision Aug 11, 1983
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
22
Review Days
55

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Basic Information

Device Name
HR 100T
K Number
K831955
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2780
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Thought Technology , Ltd.
Date Received
June 17, 1983
Decision Date
August 11, 1983
Product Code
JOM
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
JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

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Other Clearances by Thought Technology , Ltd.

K Number Device Name
K213197 MyOnyx System
K201014 MyOnyx System
K053434 MYOTRAC INFINITI ELECTRICAL STIMULATOR
K053266 MYOTRAC INFINITI
K925681 MYOTRAC2D/CS
K932149 THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE
K935213 INCONTROL
K915858 MYOTRAC2
K915859 MYOTRAC/S, MYODAC/S
K913898 MYOTRAC+/S, MYODAC+/S
Search all 22 clearances from Thought Technology , Ltd. →