PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K891972
Substantially EquivalentGrandtech Rubber Products Co. , Ltd.
FDA 510(k) clearance K891972 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-05-12. Applicant: Grandtech Rubber Products Co. , Ltd.. Device class: 1.
Clearance details
- Applicant
- Grandtech Rubber Products Co. , Ltd.
- 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
- Hong Kong, HK
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Data sourced from openFDA. This site is unofficial and independent of the FDA.