SICKLE-2000— 510(k) K955719
Substantially EquivalentMedicus Technologies, Inc.
FDA 510(k) clearance K955719 for SICKLE-2000, Substantially Equivalent on 1996-08-14. Applicant: Medicus Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Medicus Technologies, Inc.
- Product code
- Code GIQ
- Device class
- Class 2
- Regulation
- 21 CFR 864.7415
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- West Chester, PA, US
Recent devices under product code GIQ
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