LATEX PATIENT EXAMINATION GLOVES— 510(k) K894774
Substantially EquivalentAmerican Rubber Industries
FDA 510(k) clearance K894774 for LATEX PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1989-08-24. Applicant: American Rubber Industries. Device class: 1.
Clearance details
- Applicant
- American Rubber Industries
- 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
- San Diego, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.