LEGIONELLA PNEUMOPHILA— 510(k) K822066
Substantially EquivalentBiodan Medical Systems, Ltd.
FDA 510(k) clearance K822066 for LEGIONELLA PNEUMOPHILA, Substantially Equivalent on 1982-09-21. Applicant: Biodan Medical Systems, Ltd.. Device class: 2.
Clearance details
- Applicant
- Biodan Medical Systems, Ltd.
- Product code
- Code LHL
- Device class
- Class 2
- Regulation
- 21 CFR 866.3300
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Israel, IL
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More clearances from Biodan Medical Systems, Ltd.
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