LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED— 510(k) K982901
Substantially EquivalentVitalcare Group, Inc.
FDA 510(k) clearance K982901 for LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED, Substantially Equivalent on 1998-12-21. Applicant: Vitalcare Group, Inc.. Device class: 1.
Clearance details
- Applicant
- Vitalcare Group, 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
- Miami, FL, US
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More clearances from Vitalcare Group, Inc.
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