TELECTRONICS MODEL 2401
FDA 510(k) clearance K831697 · decided 1984-09-04
Clearance details
- K-number
- K831697
- Device name
- TELECTRONICS MODEL 2401
- Applicant
- Seamed Corp.
- Decision
- Substantially Equivalent
- Date received
- 1983-05-25
- Decision date
- 1984-09-04
- Days to decision
- 468 days
- Clearance type
- Traditional
- Product code
- DTC
- Device class
- 2
- Regulation number
- 870.3630
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
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| EXTERNAL PACEMAKER ANALYZER MODEL PMA-1 (K903966) | Bio-Tek Instruments, Inc. | 1991-06-19 |
| MODEL 5311B A-V PACING SYSTEM ANALYZER (K910595) | Medtronic Vascular | 1991-05-07 |
| CPI MODEL 2215/SEAMED MODEL 3400 (K910223) | Seamed Corp. | 1991-03-19 |
| PK-55 ANDOVER MEDICAL PART #5455 LABEL CHANGE (K901332) | Biotronik, GmbH & Co. | 1990-05-09 |
| MEDTRONIC MODEL 5401B TEST CABLE (K896632) | Medtronic Vascular | 1989-12-13 |
| MEDTRONIC MODEL 5311B A-V PACING SYSTEM ANALYZER (K884331) | Medtronic Vascular | 1989-01-10 |
| PACER SENSING ANALYZER (PSA 100) (K882327) | Oscor Medical Corp. | 1988-10-06 |
Recalls involving this device
No recalls on record reference this clearance.