510(k) K791801

CONPHAR FINGERTIP SUCTION CONTROL by Conphar, Inc. — Product Code JOL

K791801 is an FDA 510(k) premarket notification submitted by Conphar, Inc. for the device "CONPHAR FINGERTIP SUCTION CONTROL". The FDA issued a decision of Substantially Equivalent on Sep 21, 1979. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Conphar, Inc. has 121 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Sep 21, 1979
Date Received
Sep 13, 1979
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
510(k) Exempt

Source: FDA 510(k) database entry for K791801. Report a data issue: hello@regdatalab.com.