CAPILLARY TUBE, BLOOD COLLECTION— 510(k) K885138
Substantially EquivalentCoeur Laboratories, Inc.
FDA 510(k) clearance K885138 for CAPILLARY TUBE, BLOOD COLLECTION, Substantially Equivalent on 1989-02-07. Applicant: Coeur Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- Coeur Laboratories, Inc.
- Product code
- Code GIO
- Device class
- Class 1
- Regulation
- 21 CFR 864.6150
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raleigh, NC, US
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