FDA 510(k)
FDA class 3
Substantially Equivalent
🇺🇸 United States
MODELS 5976/5977 PACEMAKER PULSE GENER
K Number: K810677
·
Decision May 27, 1981
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
460
Applicant Total
209
Review Days
75
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Basic Information
- Device Name
- MODELS 5976/5977 PACEMAKER PULSE GENER
- K Number
- K810677
- Device Class
- FDA class 3
- Clearance Type
- Traditional
- Regulation Number
- 870.3610
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Medtronic, Inc.
- Date Received
- March 13, 1981
- Decision Date
- May 27, 1981
- 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 |
Similar 510(k) Clearances
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