LA ANTIBODY TEST KIT— 510(k) K874195
Substantially EquivalentLipogen, Inc.
FDA 510(k) clearance K874195 for LA ANTIBODY TEST KIT, Substantially Equivalent on 1988-03-11. Applicant: Lipogen, Inc.. Device class: 2.
Clearance details
- Applicant
- Lipogen, Inc.
- Product code
- Code LJM
- Device class
- Class 2
- Regulation
- 21 CFR 866.5100
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Knoxville, TN, US
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