LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDERED)— 510(k) K991949
Substantially EquivalentLa Glove (M) Sdn. Bhd.
FDA 510(k) clearance K991949 for LAGLOVE BRAND NITRILE SURGICAL GLOVE-STERILE (POWDERED), Substantially Equivalent on 1999-08-12. Applicant: La Glove (M) Sdn. Bhd.. Device class: 1.
Clearance details
- Applicant
- La Glove (M) Sdn. Bhd.
- Product code
- Code KGO
- Device class
- Class 1
- Regulation
- 21 CFR 878.4460
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Selangor Darul Ehsan Mala, MG
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Data sourced from openFDA. This site is unofficial and independent of the FDA.