WAKO L-TYPE FE, WAKO L-TYPE CALIBRATOR— 510(k) K984119
Substantially EquivalentWako Chemicals USA, Inc.
FDA 510(k) clearance K984119 for WAKO L-TYPE FE, WAKO L-TYPE CALIBRATOR, Substantially Equivalent on 1999-01-15. Applicant: Wako Chemicals USA, Inc.. Device class: 1.
Clearance details
- Applicant
- Wako Chemicals USA, Inc.
- Product code
- Code CFM
- Device class
- Class 1
- Regulation
- 21 CFR 862.1410
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Richmond, VA, US
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