NEUTRASAL
FDA 510(k) clearance K091718 · decided 2009-09-02
Clearance details
- K-number
- K091718
- Device name
- NEUTRASAL
- Applicant
- Bartor Pharmacal Co., Inc.
- Decision
- Substantially Equivalent
- Date received
- 2009-06-11
- Decision date
- 2009-09-02
- Days to decision
- 83 days
- Clearance type
- Traditional
- Product code
- LFD
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Pomona, NY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.