510(k) K872917

JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER by American Pharmaseal Div. Ahsc — Product Code BSY

K872917 is an FDA 510(k) premarket notification submitted by American Pharmaseal Div. Ahsc for the device "JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER". The FDA issued a decision of Substantially Equivalent on August 11, 1987. The device falls under product code BSY (Catheters, Suction, Tracheobronchial), a Class I device regulated under 21 CFR 868.6810. American Pharmaseal Div. Ahsc has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 11, 1987
Date Received
July 27, 1987
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