LATEX PATIENT EXAMINATION GLOVES— 510(k) K911081
Substantially EquivalentMedical Device Inspection Co., Inc.
FDA 510(k) clearance K911081 for LATEX PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1991-03-21. Applicant: Medical Device Inspection Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Medical Device Inspection Co., Inc.
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
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More clearances from Medical Device Inspection Co., Inc.
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