A.C.T. III

Culture Media, Non-propagating Transport

REMEL CO.

The following data is part of a premarket notification filed by Remel Co. with the FDA for A.c.t. Iii.

Pre-market Notification Details

Device IDK965151
510k NumberK965151
Device Name:A.C.T. III
ClassificationCulture Media, Non-propagating Transport
Applicant REMEL CO. 12076 SANTA FE DR. Lenexa,  KS  66215
ContactMary Ann Silvius
CorrespondentMary Ann Silvius
REMEL CO. 12076 SANTA FE DR. Lenexa,  KS  66215
Product CodeJSM  
CFR Regulation Number866.2390 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-12-23
Decision Date1997-01-22

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