DISPOSABLE LATEX PATIENT EXAMINATION GLOVES— 510(k) K951670
Substantially EquivalentEmi Groups (U.S.A.), Inc.
FDA 510(k) clearance K951670 for DISPOSABLE LATEX PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1995-06-15. Applicant: Emi Groups (U.S.A.), Inc.. Device class: 1.
Clearance details
- Applicant
- Emi Groups (U.S.A.), 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
- Alhambra, CA, US
Recent devices under product code LYY
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Data sourced from openFDA. This site is unofficial and independent of the FDA.