510(k) K001662

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

K001662 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 August 2, 2000. 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
August 2, 2000
Date Received
May 31, 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