DERMAGRIP POWDER FREE BLUE NITRILE EXAMINATION GLOVE, NON STERILE— 510(k) K990750
Substantially EquivalentWrp Specialty Products Sdn. Bhd.
FDA 510(k) clearance K990750 for DERMAGRIP POWDER FREE BLUE NITRILE EXAMINATION GLOVE, NON STERILE, Substantially Equivalent on 1999-10-15. Applicant: Wrp Specialty Products Sdn. Bhd.. Device class: 1.
Clearance details
- Applicant
- Wrp Specialty Products Sdn. Bhd.
- Product code
- Code LZA
- 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 Daurl Ehsan, Sepang, MY
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More clearances from Wrp Specialty Products Sdn. Bhd.
view all- K032016 — DERMAGRIP-X POWDER FREE LATEX EXAMINATION GLOVES COATED WITH ALPHA LIPOIC ACID AND VITAMIN E, AND WITH PROTEIN CONTENT
- K022808 — DERMAGRIP POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE WITH PROTEIN CONTENT LABELING CLAIM (50 UG OR LESS)
- K021561 — DERMAGRIP AND MULTIPLE POWDER FREE LATEX EXAMINATION GLOVES, STERILE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAM O
- K021536 — DERMAGRIP AND MULTIPLE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGR
- K021396 — DERMAGRIP AND MULTIPLE POWDER FREE PURPLE NITRILE EXAMINATION GLOVES, NON-STERILE
Adverse events under product code LZA
product code LZA- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.