BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117— 510(k) K022660
Substantially EquivalentBiocheck, Inc.
FDA 510(k) clearance K022660 for BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117, Substantially Equivalent on 2002-12-19. Applicant: Biocheck, Inc.. Device class: 2.
Clearance details
- Applicant
- Biocheck, Inc.
- Product code
- Code DRR
- Device class
- Class 2
- Regulation
- 21 CFR 870.2050
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Northridge, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.