510(k) K781866

CANNULA CADDY by Katena Products, Inc.

K781866 is an FDA 510(k) premarket notification submitted by Katena Products, Inc. for the device "CANNULA CADDY". The FDA issued a decision of Substantially Equivalent on November 15, 1978. Katena Products, Inc. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 15, 1978
Date Received
November 3, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No