FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PEFECT SHOT
K Number: K972019
·
Decision Jul 3, 1997
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
281
Applicant Total
19
Review Days
32
Basic Information
- Device Name
- PEFECT SHOT
- K Number
- K972019
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.6640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- INTERNATIONAL IMAGING ELECTRONICS
- Date Received
- June 1, 1997
- Decision Date
- July 3, 1997
- Product Code
- EIA
- 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 |
|---|---|---|---|
| EIA | Unit, Operative Dental | FDA class 1 | Dental |
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