MATANG POWDERED LATEX PATIENT EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (50 MICROGRAM OR LESS— 510(k) K000985
Substantially EquivalentMatang Mfg. Sdn. Bhd.
FDA 510(k) clearance K000985 for MATANG POWDERED LATEX PATIENT EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (50 MICROGRAM OR LESS, Substantially Equivalent on 2000-04-24. Applicant: Matang Mfg. Sdn. Bhd.. Device class: 1.
Clearance details
- Applicant
- Matang Mfg. 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
- Alexandria, VA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.