FDA 510(k)
FDA class 1
Substantially Equivalent
🇩🇪 Germany
STECO-TITANMAGNETICS
K Number: K990979
·
Decision Sep 3, 1999
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
23
Applicant Total
1
Review Days
164
Basic Information
- Device Name
- STECO-TITANMAGNETICS
- K Number
- K990979
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.3165
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Steco-System-Technik GmbH & Cokg
- Date Received
- March 23, 1999
- Decision Date
- September 3, 1999
- Product Code
- EGG
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- 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 |
|---|---|---|---|
| EGG | Attachment, Precision, All | FDA class 1 | Dental |
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