FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PROPHY PASTE
K Number: K771401
·
Decision Aug 22, 1977
Classifications
1
FEI Numbers
142
Registration Numbers
142
Same Product Code
76
Applicant Total
20
Review Days
24
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Basic Information
- Device Name
- PROPHY PASTE
- K Number
- K771401
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.6030
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- L.D. Caulk Co.
- Date Received
- July 29, 1977
- Decision Date
- August 22, 1977
- Product Code
- EJR
- 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 |
|---|---|---|---|
| EJR | Agent, Polishing, Abrasive, Oral Cavity | FDA class 1 | Dental |
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Other Clearances by L.D. Caulk Co.
| K Number | Device Name | ||
|---|---|---|---|
| K802262 | COMPOSITE RESTORATIVE | Sep 16, 1980 | Unknown |
| K801690 | VALIANT | Aug 13, 1980 | Substantially Equivalent |
| K790586 | CHEMBOND | May 16, 1979 | Substantially Equivalent |
| K790585 | FINESSE | May 16, 1979 | Substantially Equivalent |
| K780560 | DENTAL AMALGAMATOR | Apr 21, 1978 | Substantially Equivalent |
| K780384 | IMPROVED DYCAL | Mar 15, 1978 | Substantially Equivalent |
| K780301 | CAULK TYLOK | Feb 28, 1978 | Substantially Equivalent |
| K771398 | SHELL VENEER | Aug 26, 1977 | Substantially Equivalent |
| K771402 | NUVA-COTE (MODIFICATION TO) | Aug 26, 1977 | Substantially Equivalent |
| K771399 | LIP & CHEEK RETRACTOR | Aug 26, 1977 | Substantially Equivalent |