ADAPTER, CORDIS— 510(k) K770478
Substantially EquivalentCordis Corp.
FDA 510(k) clearance K770478 for ADAPTER, CORDIS, Substantially Equivalent on 1977-03-30. Applicant: Cordis Corp.. Device class: 2.
Clearance details
- Applicant
- Cordis Corp.
- Product code
- Code DTD
- Device class
- Class 2
- Regulation
- 21 CFR 870.3620
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.