510(k) K871737

CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR by Currie Medical Specialties, Inc. — Product Code BZA

K871737 is an FDA 510(k) premarket notification submitted by Currie Medical Specialties, Inc. for the device "CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR". The FDA issued a decision of Substantially Equivalent on June 22, 1987. The device falls under product code BZA (Connector, Airway (Extension)), a Class I device regulated under 21 CFR 868.5810. Currie Medical Specialties, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 22, 1987
Date Received
May 5, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Connector, Airway (Extension)
Device Class
Class I
Regulation Number
868.5810
Review Panel
AN
Submission Type