RINSENDO
FDA 510(k) clearance K052271 · decided 2006-05-26
Clearance details
- K-number
- K052271
- Device name
- RINSENDO
- Applicant
- Air Techniques, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2005-08-19
- Decision date
- 2006-05-26
- Days to decision
- 280 days
- Clearance type
- Traditional
- Product code
- NYL
- Device class
- 1
- Regulation number
- 872.4200
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Hicksville, NY, US
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
| PS System (K211721) | Inter-Med, Inc. | 2021-12-02 |
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| VATEA ENDONTIC IRRIGATION SYSTEM (K100606) | Redent Nova, Ltd. | 2010-05-28 |
Recalls involving this device
No recalls on record reference this clearance.