FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SANODENT DOUBLE-ENDED INTERDENTAL CLEAN
K Number: K832949
·
Decision Oct 4, 1983
Classifications
1
FEI Numbers
124
Registration Numbers
125
Same Product Code
14
Applicant Total
2
Review Days
32
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Basic Information
- Device Name
- SANODENT DOUBLE-ENDED INTERDENTAL CLEAN
- K Number
- K832949
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 872.6650
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- Coopercare, Inc.
- Date Received
- September 2, 1983
- Decision Date
- October 4, 1983
- Product Code
- JET
- 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 |
|---|---|---|---|
| JET | Pick, Massaging | FDA class 1 | Dental |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JET), ordered by most recent decision date.
REACH STIM-U-DENT PLAQUE REMOVERS WITH MICRODENT/REACH FLOSS STIKS WITH MICRODENT/REACH FLOSS PICS WITH MICRODENT ETC.
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GUM MASSAGER
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MASSAGING PICK FOR ORAL HYGIENE
FDA 510(k)
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PLAKOF
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Other Clearances by Coopercare, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K834283 | DENTSPLY G-106 CAVITRON ULTRASONIC | Mar 16, 1984 | Substantially Equivalent |