17-HYDROXYPROGESTERONE TEST SET— 510(k) K771729
Substantially EquivalentWien Laboratories, Inc.
FDA 510(k) clearance K771729 for 17-HYDROXYPROGESTERONE TEST SET, Substantially Equivalent on 1977-10-21. Applicant: Wien Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- Wien Laboratories, Inc.
- Product code
- Code JLX
- Device class
- Class 1
- Regulation
- 21 CFR 862.1395
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Wien Laboratories, Inc.
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