510(k) K003467

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

K003467 is an FDA 510(k) premarket notification submitted by Chase Medical, Inc. for the device "CHASE CARDIOVASCULAR PATCH". The FDA issued a decision of Substantially Equivalent on January 29, 2001. 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
January 29, 2001
Date Received
November 8, 2000
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