PATIENT EXAMINATION GLOVE— 510(k) K890592
Substantially EquivalentAlfaseal Sdn. Bhd.
FDA 510(k) clearance K890592 for PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1989-05-22. Applicant: Alfaseal Sdn. Bhd.. Device class: 1.
Clearance details
- Applicant
- Alfaseal 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
- Meru Klang Sl, MY
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More clearances from Alfaseal Sdn. Bhd.
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