CIDEX ACTIVATED DIALDEHYDE SOLUTION— 510(k) K060618
Substantially EquivalentJohnson & Johnson Co.
FDA 510(k) clearance K060618 for CIDEX ACTIVATED DIALDEHYDE SOLUTION, Substantially Equivalent on 2006-04-12. Applicant: Johnson & Johnson Co.. Device class: 2.
Clearance details
- Applicant
- Johnson & Johnson Co.
- Product code
- Code MED
- Device class
- Class 2
- Regulation
- 21 CFR 880.6885
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Irvin, CA, US
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Recalls naming K060618
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 K060618.
Data sourced from openFDA. This site is unofficial and independent of the FDA.