FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FIBER MESH
K Number: K854977
·
Decision Feb 20, 1986
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
6
Review Days
70
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Basic Information
- Device Name
- FIBER MESH
- K Number
- K854977
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Pulpdent Corp. of America
- Date Received
- December 12, 1985
- Decision Date
- February 20, 1986
- Product Code
- DZE
- 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 |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | FDA class 2 | Dental |
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Other Clearances by Pulpdent Corp. of America
| K Number | Device Name | ||
|---|---|---|---|
| K882576 | ACID ETCH GEL | Jul 15, 1988 | Substantially Equivalent |
| K863834 | EVIDENT MARK 2 APEX LOCATOR | Feb 6, 1987 | Substantially Equivalent |
| K844446 | BISICO SL(PUTTY) BISICO S2(REGULAR) S3 HEAVY ETC. | Oct 29, 1985 | Substantially Equivalent |
| K853447 | POLYCARB WATER SET | Oct 16, 1985 | Substantially Equivalent |
| K810545 | PCA PERIOCARE PERIODONTAL DRESSING | Mar 24, 1981 | Substantially Equivalent |