DADE TDM CONTROL— 510(k) K883190
Substantially EquivalentBaxter Healthcare Corp
FDA 510(k) clearance K883190 for DADE TDM CONTROL, Substantially Equivalent on 1988-09-09. Applicant: Baxter Healthcare Corp. Device class: 1.
Clearance details
- Applicant
- Baxter Healthcare Corp
- Product code
- Code DIF
- Device class
- Class 1
- Regulation
- 21 CFR 862.3280
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.