FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
POST TRAY
K Number: K863836
·
Decision Oct 14, 1986
Classifications
1
FEI Numbers
317
Registration Numbers
317
Same Product Code
15
Applicant Total
1
Review Days
14
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Basic Information
- Device Name
- POST TRAY
- K Number
- K863836
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.6880
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Market Masters, Inc.
- Date Received
- September 30, 1986
- Decision Date
- October 14, 1986
- Product Code
- EHY
- 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 |
|---|---|---|---|
| EHY | Tray, Impression, Preformed | FDA class 1 | Dental |
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