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

PORTABLE MEDICAL TABLE

K Number: K812791 · Decision Nov 24, 1981
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
30
Applicant Total
1
Review Days
49

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Basic Information

Device Name
PORTABLE MEDICAL TABLE
K Number
K812791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Richard D. Spradlin
Date Received
October 6, 1981
Decision Date
November 24, 1981
Product Code
KXJ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
KXJ Table, Radiologic

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