CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS— 510(k) K893754
Substantially EquivalentBd Becton Dickinson Vacutainer Systems Preanalytic
FDA 510(k) clearance K893754 for CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS, Substantially Equivalent on 1989-07-14. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.
Clearance details
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
- Product code
- Code JTN
- Device class
- Class 2
- Regulation
- 21 CFR 866.1620
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Franklin Lakes, NJ, US
Recent devices under product code JTN
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view allRecalls naming K893754
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K893754.
Data sourced from openFDA. This site is unofficial and independent of the FDA.