FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION OF NOGA
K Number: K990494
·
Decision Sep 3, 1999
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
429
Applicant Total
1
Review Days
198
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Basic Information
- Device Name
- MODIFICATION OF NOGA
- K Number
- K990494
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.1425
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Biosense, Inc.
- Date Received
- February 17, 1999
- Decision Date
- September 3, 1999
- Product Code
- DQK
- 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 |
|---|---|---|---|
| DQK | Computer, Diagnostic, Programmable | FDA class 2 | Cardiovascular |
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