510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
Data Acquisition Software
STRATEC Biomedical UK Limited
The following data is part of a premarket notification filed by Stratec Biomedical Uk Limited with the FDA for 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.s. Food & Drug Administration Follow Fda En Español Search Fda Home Food Drugs Medical Devices .
Pre-market Notification Details
Device ID
BK160113
510k Number
BK160113
Device Name:
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
Classification
Data Acquisition Software
Applicant
STRATEC Biomedical UK Limited 98 Main Street suite 205 Southington, CT 06489