510(k) K892441

KENDALL CURITY SUCTION CATHETERS by The Kendal Co. — Product Code BSY

K892441 is an FDA 510(k) premarket notification submitted by The Kendal Co. for the device "KENDALL CURITY SUCTION CATHETERS". The FDA issued a decision of Substantially Equivalent on May 31, 1989. The device falls under product code BSY (Catheters, Suction, Tracheobronchial), a Class I device regulated under 21 CFR 868.6810. The Kendal Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 31, 1989
Date Received
April 10, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheters, Suction, Tracheobronchial
Device Class
Class I
Regulation Number
868.6810
Review Panel
AN
Submission Type