PANOSOL 2000 624-404

Light, Ultraviolet, Dermatological

NATIONAL BIOLOGICAL CORP.

The following data is part of a premarket notification filed by National Biological Corp. with the FDA for Panosol 2000 624-404.

Pre-market Notification Details

Device IDK872707
510k NumberK872707
Device Name:PANOSOL 2000 624-404
ClassificationLight, Ultraviolet, Dermatological
Applicant NATIONAL BIOLOGICAL CORP. 1532 ENTERPRISE PKWY. Twinsburg,  OH  44087
ContactArthur Goddard
CorrespondentArthur Goddard
NATIONAL BIOLOGICAL CORP. 1532 ENTERPRISE PKWY. Twinsburg,  OH  44087
Product CodeFTC  
CFR Regulation Number878.4630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-07-07
Decision Date1987-07-27

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