The following data is part of a premarket notification filed by Seamed Corp. with the FDA for Seamed Model 6000.
| Device ID | K843807 |
| 510k Number | K843807 |
| Device Name: | SEAMED MODEL 6000 |
| Classification | Pulse-generator, Pacemaker, External |
| Applicant | SEAMED CORP. 4500-150TH. AVENUE NE Redmond, WA 98052 |
| Contact | Willilam J Evans |
| Correspondent | Willilam J Evans SEAMED CORP. 4500-150TH. AVENUE NE Redmond, WA 98052 |
| Product Code | DTE |
| CFR Regulation Number | 870.3600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-09-27 |
| Decision Date | 1985-02-01 |