510(k) K790436
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