Skip to content
Scan

Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K140307

ENVOY GUIDING CATHETER · Codman & Shurtleff, Inc. · decided 2014-04-21 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ENVOY778-248-90Cerenovus, Inc.DQY10886704074946
ENVOY778-254-00Cerenovus, Inc.DQY10886704074847
ENVOY778-248-00BCerenovus, Inc.DQY10886704074830
ENVOY778-252-90Cerenovus, Inc.DQY10886704075035
ENVOY778-256-90Cerenovus, Inc.DQY10886704074984
ENVOY778-258-90BCerenovus, Inc.DQY10886704075011
ENVOY778-254-90Cerenovus, Inc.DQY10886704074960
ENVOY778-260-90Cerenovus, Inc.DQY10886704075042
ENVOY778-258-00Cerenovus, Inc.DQY10886704074885
ENVOY778-256-00BCerenovus, Inc.DQY10886704074878
ENVOY778-252-90BCerenovus, Inc.DQY10886704075028
ENVOY778-252-00BCerenovus, Inc.DQY10886704074908
ENVOY778-254-00BCerenovus, Inc.DQY10886704074854
ENVOY778-256-90BCerenovus, Inc.DQY10886704074991
ENVOY778-256-00Cerenovus, Inc.DQY10886704074861
ENVOY778-248-00Cerenovus, Inc.DQY10886704074823
ENVOY778-260-00BCerenovus, Inc.DQY10886704074939
ENVOY778-260-90BCerenovus, Inc.DQY10886704075059
ENVOY778-258-90Cerenovus, Inc.DQY10886704075004
ENVOY778-252-00Cerenovus, Inc.DQY10886704074915
ENVOY778-260-00Cerenovus, Inc.DQY10886704074922
ENVOY778-254-90BCerenovus, Inc.DQY10886704074977
ENVOY778-248-90BCerenovus, Inc.DQY10886704074953