VERSA LITE

Light, Ultraviolet, Dermatological

DIOMEDICS, INC.

The following data is part of a premarket notification filed by Diomedics, Inc. with the FDA for Versa Lite.

Pre-market Notification Details

Device IDK073503
510k NumberK073503
Device Name:VERSA LITE
ClassificationLight, Ultraviolet, Dermatological
Applicant DIOMEDICS, INC. 24372 MCCLOUD CT. Laguna Niguel,  CA  92677
ContactGary Mocnik
CorrespondentGary Mocnik
DIOMEDICS, INC. 24372 MCCLOUD CT. Laguna Niguel,  CA  92677
Product CodeFTC  
CFR Regulation Number878.4630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-12-13
Decision Date2008-01-23

Trademark Results [VERSA LITE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERSA LITE
VERSA LITE
74293379 not registered Dead/Abandoned
Pelican Products, Inc.
1992-07-13
VERSA LITE
VERSA LITE
73588603 1485184 Dead/Cancelled
VISTA MANUFACTURING, INC.
1986-03-17

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