PROGESTERONE DIRECT RIA KIT-RADIOIMM— 510(k) K841333
Substantially EquivalentBiotecx Laboratories, Inc.
FDA 510(k) clearance K841333 for PROGESTERONE DIRECT RIA KIT-RADIOIMM, Substantially Equivalent on 1984-05-02. Applicant: Biotecx Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- Biotecx Laboratories, Inc.
- Product code
- Code JLS
- Device class
- Class 1
- Regulation
- 21 CFR 862.1620
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code JLS
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