510(k) K941232

THORA-CATH by Gesco Intl., Inc. — Product Code JOL

K941232 is an FDA 510(k) premarket notification submitted by Gesco Intl., Inc. for the device "THORA-CATH". The FDA issued a decision of Substantially Equivalent on May 11, 1994. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Gesco Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 11, 1994
Date Received
March 15, 1994
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