Submission Details
| 510(k) Number | K211927 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 22, 2021 |
| Decision Date | October 12, 2021 |
| Days to Decision | 112 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
K211927 is an FDA 510(k) clearance for the Nitrile examination gloves, a Polymer Patient Examination Glove (Class I — General Controls, product code LZA), submitted by Fitone Latex Products Co., Ltd. Guangdong (Zhanjiang, CN). The FDA issued a Cleared decision on October 12, 2021, 112 days after receiving the submission on June 22, 2021. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.6250.
| 510(k) Number | K211927 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 22, 2021 |
| Decision Date | October 12, 2021 |
| Days to Decision | 112 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | LZA — Polymer Patient Examination Glove |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 880.6250 |
| Definition | A Nitrile (or Polymer) Patient Examination Glove Is A Disposable Device Made Of Nitrile Rubber Or Synthetic Polymers That May Or May Not Bear A Trace Amount Of Residual Powder, And Is Intended To Be Worn On The Hand For Medical Purposes To Provide A Barrier Against Potentially Infectious Materials And Other Contaminants. |