FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DENSCO PROPHY ANGLE
K Number: K821686
·
Decision Jun 25, 1982
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
72
Applicant Total
4
Review Days
17
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- DENSCO PROPHY ANGLE
- K Number
- K821686
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4200
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Teledyne Densco
- Date Received
- June 8, 1982
- Decision Date
- June 25, 1982
- Product Code
- EGS
- 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 |
|---|---|---|---|
| EGS | Handpiece, Contra- And Right-Angle Attachment, Dental | FDA class 1 | Dental |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (EGS), ordered by most recent decision date.
Disposable Prophy Angle (3399-60, 3399-090, 3399-105)
FDA 510(k)
FDA Class 1
·Dental
Disposable Prophy Angle
FDA 510(k)
FDA Class 1
·Dental
Star E900 Handpiece Series
FDA 510(k)
FDA Class 1
·Dental
General Cutting Straight
FDA 510(k)
FDA Class 1
·Dental
FX Contra
FDA 510(k)
FDA Class 1
·Dental
Smooth Drive contra angle and straight handpieces
FDA 510(k)
FDA Class 1
·Dental