The following data is part of a premarket notification filed by Arco Medical Products Co. with the FDA for Implantable Heart Lead Terminal Adapter.
Device ID | K790436 |
510k Number | K790436 |
Device Name: | IMPLANTABLE HEART LEAD TERMINAL ADAPTER |
Classification | Pacemaker Lead Adaptor |
Applicant | ARCO MEDICAL PRODUCTS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DTD |
CFR Regulation Number | 870.3620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-03-07 |
Decision Date | 1979-05-14 |