FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
PRESSX ZR
K Number: K070772
·
Decision Apr 30, 2007
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
45
Review Days
40
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Basic Information
- Device Name
- PRESSX ZR
- K Number
- K070772
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.6660
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Wieland Dental + Technik GmbH & Co. KG
- Date Received
- March 21, 2007
- Decision Date
- April 30, 2007
- Product Code
- EIH
- 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 |
|---|---|---|---|
| EIH | Powder, Porcelain | FDA class 2 | Dental |
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