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.. Device class: 2.
Clearance details
- Applicant
- Allen Medical Instruments Corp.
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newport Beach, CA, US
Recent devices under product code DQD
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