510(k) K020233

CHASE CARDIOVASCULAR PATCH KIT by Chase Medical, Inc. — Product Code DXZ

K020233 is an FDA 510(k) premarket notification submitted by Chase Medical, Inc. for the device "CHASE CARDIOVASCULAR PATCH KIT". The FDA issued a decision of Substantially Equivalent on March 14, 2002. The device falls under product code DXZ (Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene), a Class II device regulated under 21 CFR 870.3470. Chase Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 2002
Date Received
January 23, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
Device Class
Class II
Regulation Number
870.3470
Review Panel
CV
Submission Type