GEMINI E— 510(k) K993623
Substantially EquivalentAllen Medical Instruments Corp.
FDA 510(k) clearance K993623 for GEMINI E, Substantially Equivalent on 2000-06-23. Applicant: Allen Medical Instruments Corp..
Clearance details
- Applicant
- Allen Medical Instruments Corp.
- Product code
- Code DQD
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newport Beach, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.