FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KULZER TRANSLUX EC
K Number: K892456
·
Decision Jun 14, 1989
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
31
Review Days
65
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Basic Information
- Device Name
- KULZER TRANSLUX EC
- K Number
- K892456
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.6070
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Kulzer, Inc.
- Date Received
- April 10, 1989
- Decision Date
- June 14, 1989
- Product Code
- EBZ
- 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 |
|---|---|---|---|
| EBZ | Activator, Ultraviolet, For Polymerization | FDA class 2 | Dental |
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Other Clearances by Kulzer, Inc.
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|---|---|---|---|
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| K910263 | CHARISMA | Jun 3, 1991 | Substantially Equivalent |
| K910719 | SILICOATER MD | Apr 29, 1991 | Substantially Equivalent |
| K905131 | DURAFILL COLOR VS | Mar 15, 1991 | Substantially Equivalent |
| K905302 | DENTHESIVE | Feb 26, 1991 | Substantially Equivalent |
| K904555 | DURAFILL FLOW | Nov 13, 1990 | Substantially Equivalent |
| K903317 | DENTALON PLUS | Aug 13, 1990 | Substantially Equivalent |
| K902115 | PALAPRESS(R) VARIO RESIN | Jul 27, 1990 | Substantially Equivalent |
| K902350 | PALATRAY LC RESIN IMPRESSION TRAY MATERIAL | Jul 26, 1990 | Substantially Equivalent |