SCANLAN SINGLE-USE AORTA PUNCH— 510(k) K823764
Substantially EquivalentScanlan Intl., Inc.
FDA 510(k) clearance K823764 for SCANLAN SINGLE-USE AORTA PUNCH, Substantially Equivalent on 1983-03-24. Applicant: Scanlan Intl., Inc.. Device class: 1.
Clearance details
- Applicant
- Scanlan Intl., Inc.
- Product code
- Code DWS
- Device class
- Class 1
- Regulation
- 21 CFR 870.4500
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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