FERTILIZATION MEDIA-HTF

Media, Reproductive

INTL., INC.

The following data is part of a premarket notification filed by Intl., Inc. with the FDA for Fertilization Media-htf.

Pre-market Notification Details

Device IDK991173
510k NumberK991173
Device Name:FERTILIZATION MEDIA-HTF
ClassificationMedia, Reproductive
Applicant INTL., INC. 170 FORT PATH RD. UNIT 14 Madison,  CT  06443
ContactMichael D Cecchi
CorrespondentMichael D Cecchi
INTL., INC. 170 FORT PATH RD. UNIT 14 Madison,  CT  06443
Product CodeMQL  
CFR Regulation Number884.6180 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-04-07
Decision Date1999-07-19
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00815965020198 K991173 000
00815965020181 K991173 000
00815965020174 K991173 000

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