Powder Free Nitrile Examination Gloves, Colored (Green, Orange, Purple, White, & Black)— 510(k) K220859
Substantially EquivalentCareglove Global Sdn. Bhd.
FDA 510(k) clearance K220859 for Powder Free Nitrile Examination Gloves, Colored (Green, Orange, Purple, White, & Black), Substantially Equivalent on 2022-09-09. Applicant: Careglove Global Sdn. Bhd.. Device class: 1.
Clearance details
- Applicant
- Careglove Global 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
- Seremban, MY
Recent devices under product code LZA
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- K260312 — Nitrile Powder Free Examination Glove, Blue Tested for Use with 32 Chemotherapy Drugs and Fentanyl Permeation Resistance Claim +1 more
- K260794 — NON-STERILE POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WITH LICORICE ROOT EXTRACT AND UREA, TESTED FOR USE WITH CHEMOTHERAPY DRUGS, FENTANYL CITRATE, XYLAZINE HCl, AND GASTRIC ACID. OCEAN COLOR
- K262014 — PUREZERO* MARIN* Nitrile Powder-Free Exam Gloves; PUREZERO* MARIN-XTRA* Nitrile Powder-Free Exam Gloves
More clearances from Careglove Global Sdn. Bhd.
view all- K250578 — Nitrile Examination Gloves Powder Free Tested for Use With Chemotherapy Drugs & Fentanyl Citrate (Blue & Black)
- K230121 — Nitrile Examination Gloves Powder Free Tested For Use With Chemotherapy Drugs & Fentanyl Citrate (Blue & Black)
- K213993 — Powder Free Chloroprene Examination Glove Coloured (Blue, Green)
- K211666 — Powder Free Nitrile Examination Gloves, Blue Chemotest
- K190241 — Sterile Latex Surgical Glove, Powder Free
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.