510(k) K902687

STERI-CATH-DL by Concord/Portex — Product Code BSY

K902687 is an FDA 510(k) premarket notification submitted by Concord/Portex for the device "STERI-CATH-DL". The FDA issued a decision of Substantially Equivalent on August 29, 1990. The device falls under product code BSY (Catheters, Suction, Tracheobronchial), a Class I device regulated under 21 CFR 868.6810. Concord/Portex has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 1990
Date Received
June 19, 1990
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