510(k) K790436

IMPLANTABLE HEART LEAD TERMINAL ADAPTER by Arco Medical Products Co. — Product Code DTD

K790436 is an FDA 510(k) premarket notification submitted by Arco Medical Products Co. for the device "IMPLANTABLE HEART LEAD TERMINAL ADAPTER". The FDA issued a decision of Substantially Equivalent on May 14, 1979. The device falls under product code DTD (Pacemaker Lead Adaptor), a Class II device regulated under 21 CFR 870.3620. Arco Medical Products Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 14, 1979
Date Received
March 7, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pacemaker Lead Adaptor
Device Class
Class II
Regulation Number
870.3620
Review Panel
CV
Submission Type