D903 AVANT ADULT HOLLOW FIBER OXYGENATOR— 510(k) K980600
Substantially EquivalentDideco S.P.A.
FDA 510(k) clearance K980600 for D903 AVANT ADULT HOLLOW FIBER OXYGENATOR, Substantially Equivalent on 1998-08-12. Applicant: Dideco S.P.A.. Device class: 2.
Clearance details
- Applicant
- Dideco S.P.A.
- Product code
- Code JOW
- Device class
- Class 2
- Regulation
- 21 CFR 870.5800
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Attleboro, MA, US
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