DELFIA(R) 17 -OH-PROGESTERON KIT— 510(k) K912026
Substantially EquivalentPharmacia Diagnostics, Inc.
FDA 510(k) clearance K912026 for DELFIA(R) 17 -OH-PROGESTERON KIT, Substantially Equivalent on 1991-06-25. Applicant: Pharmacia Diagnostics, Inc.. Device class: 1.
Clearance details
- Applicant
- Pharmacia Diagnostics, 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
- Columbia, MD, US
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More clearances from Pharmacia Diagnostics, Inc.
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