EPC FILTER— 510(k) K813123
Substantially EquivalentCodman & Shurtleff, Inc.
FDA 510(k) clearance K813123 for EPC FILTER, Substantially Equivalent on 1981-11-27. Applicant: Codman & Shurtleff, Inc.. Device class: 2.
Clearance details
- Applicant
- Codman & Shurtleff, Inc.
- Product code
- Code DRR
- Device class
- Class 2
- Regulation
- 21 CFR 870.2050
- 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.