AFP CARDIAC PACING SYSTEM MODEL 283— 510(k) K942440
Substantially Equivalent - Subject to Tracking Reg.Siemens-Pacesetter, Inc.
FDA 510(k) clearance K942440 for AFP CARDIAC PACING SYSTEM MODEL 283, Substantially Equivalent - Subject to Tracking Reg. on 1994-08-08. Applicant: Siemens-Pacesetter, Inc..
Clearance details
- Applicant
- Siemens-Pacesetter, Inc.
- Product code
- Code DTB
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent - Subject to Tracking Reg.
- Clearance type
- Traditional
- Location
- Sylmar, CA, US
Adverse events under product code DTB
product code DTB- Death
- 1,491
- Injury
- 67,311
- Malfunction
- 79,368
- Other
- 10
- Total
- 148,180
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.