FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SIROPORT
K Number: K800172
·
Decision Feb 5, 1980
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
62
Applicant Total
66
Review Days
11
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Basic Information
- Device Name
- SIROPORT
- K Number
- K800172
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.6250
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Siemens Corp.
- Date Received
- January 25, 1980
- Decision Date
- February 5, 1980
- Product Code
- KLC
- 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 |
|---|---|---|---|
| KLC | Chair, Dental, With Operative Unit | FDA class 1 | Dental |
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ULTIMA 2 DENTAL CHAIR
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