STINGRAY DR, MODEL 1— 510(k) K992794
Substantially EquivalentInfimed, Inc.
FDA 510(k) clearance K992794 for STINGRAY DR, MODEL 1, Substantially Equivalent on 1999-11-09. Applicant: Infimed, Inc.. Device class: 2.
Clearance details
- Applicant
- Infimed, Inc.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Liverpool, NY, US
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