FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
THE PLACER
K Number: K811582
·
Decision Jul 28, 1981
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
12
Applicant Total
32
Review Days
53
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Basic Information
- Device Name
- THE PLACER
- K Number
- K811582
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.4565
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Cavitron Corp.
- Date Received
- June 5, 1981
- Decision Date
- July 28, 1981
- Product Code
- EID
- 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 |
|---|---|---|---|
| EID | Syringe, Restorative And Impression Material | FDA class 1 | Dental |
Similar 510(k) Clearances
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BONE GRAFT DELIVERY SYRINGES
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ACCESS IMPRESSION BARREL
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CAULK'S VPS CARTRIDGE SYSTEM
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COLTENE JET-MIXER
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CENTRIX RIBBON TUBES
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Other Clearances by Cavitron Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K810207 | MINOR SURGERY LIGHT | Feb 13, 1981 | Substantially Equivalent |
| K802928 | SPIROMETRIC COMPUTER #SC-10 | Dec 17, 1980 | Substantially Equivalent |
| K801623 | CAVITRON ULTRASONIC SURG. ASPIR. CUSA | Nov 18, 1980 | Substantially Equivalent |
| K801877 | SLIT LAMP ATTACHMENT | Sep 16, 1980 | Substantially Equivalent |
| K800869 | MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA | May 28, 1980 | Substantially Equivalent |
| K800722 | AUTO-FIELD D AUTOMATED VISUAL DETECTOR | Apr 29, 1980 | Substantially Equivalent |
| K791585 | MODEL G-61 ULTRASONIC DENTAL UNIT | Sep 19, 1979 | Substantially Equivalent |
| K791277 | MODEL 6500 EXTRACTION IRRIGATION SYS | Aug 22, 1979 | Substantially Equivalent |
| K782054 | LASER, CO2 SURGICAL | Jan 17, 1979 | Substantially Equivalent |
| K782065 | LASER, PHOTOCOAGULATION | Dec 28, 1978 | Substantially Equivalent |