MYOGLOBIN RIA TEST KIT— 510(k) K915233
Substantially EquivalentPro Diagnostics, Inc.
FDA 510(k) clearance K915233 for MYOGLOBIN RIA TEST KIT, Substantially Equivalent on 1992-03-30. Applicant: Pro Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Pro Diagnostics, Inc.
- Product code
- Code DDR
- Device class
- Class 2
- Regulation
- 21 CFR 866.5680
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.