LASER-DIL— 510(k) K850095
Substantially EquivalentHematology Marketing Assoc.
FDA 510(k) clearance K850095 for LASER-DIL, Substantially Equivalent on 1985-03-29. Applicant: Hematology Marketing Assoc.. Device class: 1.
Clearance details
- Applicant
- Hematology Marketing Assoc.
- Product code
- Code GIF
- Device class
- Class 1
- Regulation
- 21 CFR 864.8200
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, CA, US
Recent devices under product code GIF
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