FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ENDOVAGE SYRINGE
K Number: K792577
·
Decision Jan 4, 1980
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
15
Applicant Total
2
Review Days
21
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Basic Information
- Device Name
- ENDOVAGE SYRINGE
- K Number
- K792577
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Dental Development Services, Inc.
- Date Received
- December 14, 1979
- Decision Date
- January 4, 1980
- Product Code
- EIC
- 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 |
|---|---|---|---|
| EIC | Syringe, Periodontic, Endodontic, Irrigating | FDA class 1 | Dental |
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Other Clearances by Dental Development Services, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K792578 | EPIC CANNULA | Jan 4, 1980 | Substantially Equivalent |