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

SUNTANNING BED

K Number: K895325 · Decision Sep 15, 1989
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
80
Applicant Total
3
Review Days
17

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Basic Information

Device Name
SUNTANNING BED
K Number
K895325
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4635
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Sunbronze
Date Received
August 29, 1989
Decision Date
September 15, 1989
Product Code
LEJ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
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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Other Clearances by Sunbronze

K Number Device Name
K896983 SUNBRONZE SB24C/65 ULTRA
K896191 SUNTANNING BED, INC. T12 UVA TANNING LAMPS