LH QUIK RIA KIT— 510(k) K840174
Substantially EquivalentPacific Biotech, Inc.
FDA 510(k) clearance K840174 for LH QUIK RIA KIT, Substantially Equivalent on 1984-03-19. Applicant: Pacific Biotech, Inc.. Device class: 1.
Clearance details
- Applicant
- Pacific Biotech, Inc.
- Product code
- Product code CEP
- Device class
- Class 1
- Regulation
- 21 CFR 862.1485
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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