AQUAPLAST PALATAL STENT— 510(k) K973370
Substantially EquivalentWfr/Aquaplast Corp.
FDA 510(k) clearance K973370 for AQUAPLAST PALATAL STENT, Substantially Equivalent on 1997-12-02. Applicant: Wfr/Aquaplast Corp.. Device class: 2.
Clearance details
- Applicant
- Wfr/Aquaplast Corp.
- Product code
- Code EMA
- Device class
- Class 2
- Regulation
- 21 CFR 872.3275
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wyckoff, NJ, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.