TPK 1980/1— 510(k) K822449
Substantially EquivalentPlantex USA, Inc.
FDA 510(k) clearance K822449 for TPK 1980/1, Substantially Equivalent on 1982-10-27. Applicant: Plantex USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Plantex USA, Inc.
- Product code
- Code LCX
- Device class
- Class 2
- Regulation
- 21 CFR 862.1155
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.