K233740
- 510(k) number
- K233740
- Device name
- Black Nitrile Powder Free Patient Examination Glove, Non Sterile
- Applicant
- W.A. Rubbermate Co., Ltd. TH
- Product code
- LZA — Polymer Patient Examination Glove
- Decision date
- 2024-02-13
- Date received
- 2023-11-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233740.pdf
Official FDA record: K233740
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.