PRESSURE SORE MANAGEMENT KIT— 510(k) K912116
Substantially EquivalentMedical Device Inspection Co., Inc.
FDA 510(k) clearance K912116 for PRESSURE SORE MANAGEMENT KIT, Substantially Equivalent on 1991-10-18. Applicant: Medical Device Inspection Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Medical Device Inspection Co., Inc.
- Product code
- Code MCY
- Device class
- Class 2
- Regulation
- 21 CFR 880.5075
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
Recent devices under product code MCY
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