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

FITNESS LOGGER

K Number: K840020 · Decision Oct 26, 1984
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
17
Review Days
295

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Basic Information

Device Name
FITNESS LOGGER
K Number
K840020
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Unknown
Applicant
Britt Corp., Inc.
Date Received
January 5, 1984
Decision Date
October 26, 1984
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by Britt Corp., Inc.

K Number Device Name
K003828 VASO PRESS DVT FOOT GARMENT #VP 520
K991038 VASO PRESS DVT SYSTEM, MODELS VP500, VP501
K974393 VASO PRESS SYSTEM
K860977 MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION
K860975 MODEL 545-45 LASER FOR EAR, NOSE & THROAT
K860974 MODEL 545-45 LASER FOR DERMA., POD., SURGICAL
K860277 MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT
K860273 MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY
K860278 MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTIC
K851425 MODEL J25-25 WATT CO2 LASER
Search all 17 clearances from Britt Corp., Inc. →