PATIENT EXAMINATION GLOVE— 510(k) K890975
Substantially EquivalentKleartex Sdn Bhd
FDA 510(k) clearance K890975 for PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1989-05-11. Applicant: Kleartex Sdn Bhd. Device class: 1.
Clearance details
- Applicant
- Kleartex Sdn Bhd
- 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
- Selangor Darul Ehsan, MY
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More clearances from Kleartex Sdn Bhd
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