CARDF— 510(k) K823731
Substantially EquivalentShiley, Inc.
FDA 510(k) clearance K823731 for CARDF, Substantially Equivalent on 1983-01-05. Applicant: Shiley, Inc.. Device class: 2.
Clearance details
- Applicant
- Shiley, Inc.
- Product code
- Code DTP
- Device class
- Class 2
- Regulation
- 21 CFR 870.4230
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Shiley, Inc.
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