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

FANCY TAN SUNBED

K Number: K810366 · Decision Mar 5, 1981
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
80
Applicant Total
1
Review Days
21

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Basic Information

Device Name
FANCY TAN SUNBED
K Number
K810366
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4635
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Fancy Tan, Inc.
Date Received
February 12, 1981
Decision Date
March 5, 1981
Product Code
LEJ
Advisory Committee
General, Plastic Surgery
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
LEJ Booth, Sun Tan

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