CALIBRATION REFERENCE PLASMA— 510(k) K874940
Substantially EquivalentBaxter Healthcare Corp
FDA 510(k) clearance K874940 for CALIBRATION REFERENCE PLASMA, Substantially Equivalent on 1988-02-09. Applicant: Baxter Healthcare Corp. Device class: 2.
Clearance details
- Applicant
- Baxter Healthcare Corp
- Product code
- Code GGP
- Device class
- Class 2
- Regulation
- 21 CFR 864.7290
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
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