510(k) K770233

STERILE SUCTION CATHETER W/CONTROL by Chesire Laboratories — Product Code JOL

K770233 is an FDA 510(k) premarket notification submitted by Chesire Laboratories for the device "STERILE SUCTION CATHETER W/CONTROL". The FDA issued a decision of Substantially Equivalent on April 5, 1977. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Chesire Laboratories has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 5, 1977
Date Received
February 7, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter And Tip, Suction
Device Class
Class II
Regulation Number
880.6740
Review Panel
HO
Submission Type