LEOCOR CORFLO(TM) PUMP— 510(k) K900350
Substantially EquivalentLeocor, Inc.
FDA 510(k) clearance K900350 for LEOCOR CORFLO(TM) PUMP, Substantially Equivalent on 1990-07-17. Applicant: Leocor, Inc.. Device class: 2.
Clearance details
- Applicant
- Leocor, Inc.
- Product code
- Code DXK
- Device class
- Class 2
- Regulation
- 21 CFR 870.2330
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Webster, TX, US
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