TRIFLEX SELECT— 510(k) K070647
Substantially EquivalentCardinal Health, Inc.
FDA 510(k) clearance K070647 for TRIFLEX SELECT, Substantially Equivalent on 2007-06-22. Applicant: Cardinal Health, Inc.. Device class: 1.
Clearance details
- Applicant
- Cardinal Health, Inc.
- Product code
- Code KGO
- Device class
- Class 1
- Regulation
- 21 CFR 878.4460
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Waukegan, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.