MARKII VENTIMASKS— 510(k) K781325
Substantially EquivalentVickers America Medical Corp.
FDA 510(k) clearance K781325 for MARKII VENTIMASKS, Substantially Equivalent on 1978-09-27. Applicant: Vickers America Medical Corp.. Device class: 1.
Clearance details
- Applicant
- Vickers America Medical Corp.
- Product code
- Code BYF
- Device class
- Class 1
- Regulation
- 21 CFR 868.5600
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code BYF
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