ULTROSER G— 510(k) K844413
Substantially EquivalentLkb Instruments, Inc.
FDA 510(k) clearance K844413 for ULTROSER G, Substantially Equivalent on 1985-02-27. Applicant: Lkb Instruments, Inc.. Device class: 1.
Clearance details
- Applicant
- Lkb Instruments, Inc.
- Product code
- Code JJY
- Device class
- Class 1
- Regulation
- 21 CFR 862.1660
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gaithersburg, MD, US
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