PRESSORE MONITOR— 510(k) K954670
Substantially EquivalentCleveland Medical Devices, Inc.
FDA 510(k) clearance K954670 for PRESSORE MONITOR, Substantially Equivalent on 1995-10-30. Applicant: Cleveland Medical Devices, Inc.. Device class: 1.
Clearance details
- Applicant
- Cleveland Medical Devices, Inc.
- Product code
- Code IKE
- Device class
- Class 1
- Regulation
- 21 CFR 890.1615
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cleveland, OH, US
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