SPOTCHECK BLOOD SPOT CONTROL, ASSAYED— 510(k) K090940
Substantially EquivalentAstoria-Pacific, Inc.
FDA 510(k) clearance K090940 for SPOTCHECK BLOOD SPOT CONTROL, ASSAYED, Substantially Equivalent on 2009-12-14. Applicant: Astoria-Pacific, Inc.. Device class: 1.
Clearance details
- Applicant
- Astoria-Pacific, Inc.
- Product code
- Code JJT
- Device class
- Class 1
- Regulation
- 21 CFR 862.1660
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Clackamas, OR, US
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More clearances from Astoria-Pacific, Inc.
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- K080294 — ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE MICROPLATE REAGENT KIT
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Data sourced from openFDA. This site is unofficial and independent of the FDA.