NICALERT— 510(k) K021688
Substantially EquivalentNymox Pharmaceutical Corporation
FDA 510(k) clearance K021688 for NICALERT, Substantially Equivalent on 2002-10-18. Applicant: Nymox Pharmaceutical Corporation. Device class: 1.
Clearance details
- Applicant
- Nymox Pharmaceutical Corporation
- Product code
- Code MRS
- Device class
- Class 1
- Regulation
- 21 CFR 862.3220
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Maywood, NJ, US
Recent devices under product code MRS
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