FDA 510(k)
FDA class 3
Substantially Equivalent
🇺🇸 United States
VICOR MODELS 410B & 410D AND MODIFIED 410A PACEMA.
K Number: K881711
·
Decision May 26, 1988
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
460
Applicant Total
3
Review Days
36
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Basic Information
- Device Name
- VICOR MODELS 410B & 410D AND MODIFIED 410A PACEMA.
- K Number
- K881711
- Device Class
- FDA class 3
- Clearance Type
- Traditional
- Regulation Number
- 870.3610
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Telectronics and Cordis Pacing Systems
- Date Received
- April 20, 1988
- Decision Date
- May 26, 1988
- Product Code
- DXY
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DXY | Implantable Pacemaker Pulse-Generator | FDA class 3 | Cardiovascular |
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