UNIGLOVES— 510(k) K971731
Substantially EquivalentUni-Glove (Usa), Inc.
FDA 510(k) clearance K971731 for UNIGLOVES, Substantially Equivalent on 1997-08-05. Applicant: Uni-Glove (Usa), Inc.. Device class: 1.
Clearance details
- Applicant
- Uni-Glove (Usa), 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
- Torrance, 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.