510(k) K813435

BAXA ADLI SEAL by Baxa Corp., Sub. of Cook Group, Inc. — Product Code KPE

K813435 is an FDA 510(k) premarket notification submitted by Baxa Corp., Sub. of Cook Group, Inc. for the device "BAXA ADLI SEAL". The FDA issued a decision of Substantially Equivalent on December 18, 1981. The device falls under product code KPE (Container, I.V.), a Class II device regulated under 21 CFR 880.5025. Baxa Corp., Sub. of Cook Group, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 18, 1981
Date Received
December 8, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Container, I.V.
Device Class
Class II
Regulation Number
880.5025
Review Panel
HO
Submission Type