XENAMATIC SERIES OF XENON REBREATH DEV— 510(k) K820571
Substantially EquivalentDiversified P.A.
FDA 510(k) clearance K820571 for XENAMATIC SERIES OF XENON REBREATH DEV, Substantially Equivalent on 1982-03-31. Applicant: Diversified P.A.. Device class: 2.
Clearance details
- Applicant
- Diversified P.A.
- Product code
- Code IYT
- Device class
- Class 2
- Regulation
- 21 CFR 892.1390
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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