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

CLEO TL80W PROFESSIONAL CLEO TL80W PROFESSIONAL R, CLEO TL100 W PROFESSIONAL

K Number: K940672 · Decision Mar 18, 1994
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
80
Applicant Total
6
Review Days
30

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Basic Information

Device Name
CLEO TL80W PROFESSIONAL CLEO TL80W PROFESSIONAL R, CLEO TL100 W PROFESSIONAL
K Number
K940672
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4635
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Philips Lighting Co.
Date Received
February 16, 1994
Decision Date
March 18, 1994
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LEJ), ordered by most recent decision date.

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Other Clearances by Philips Lighting Co.

K Number Device Name
K021514 PHILIPS PLS9W/12/2P UVB
K021092 PHILIPS TL 20W/01RS UV-B, PHILIPS PL-S 9W/01/2P UV, AND PHILIPS PL-L 36W/01/4P UV-B
K935840 TL 20W/12/RS & TL 40W/12/RS
K922963 TL100W/12
K910767 TL100W/01 UVB LAMP