FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TABLE, MODELS 610,611 & 612

K Number: K834103 · Decision Jan 13, 1984
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
101
Applicant Total
35
Review Days
45

Basic Information

Device Name
TABLE, MODELS 610,611 & 612
K Number
K834103
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3760
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
TRI W-G, INC.
Date Received
November 29, 1983
Decision Date
January 13, 1984
Product Code
INQ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
INQ Table, Powered

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