Submission Details
| 510(k) Number | K193581 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | December 23, 2019 |
| Decision Date | March 20, 2020 |
| Days to Decision | 88 days |
| Submission Type | Abbreviated |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
K193581 is an FDA 510(k) clearance for the Non-Sterile, Powder Free Nitrile Exam Glove Tested for use with Chemotherapy Drugs - Lilac, Non-Sterile, Powder Free Nitrile Exam Glove Tested for use with Chemotherapy Drugs - Orchid, Non-Sterile, Powder Free Nitrile Exam Glove Tested for use with Chemotherapy Drugs - Oyster, a Polymer Patient Examination Glove (Class I — General Controls, product code LZA), submitted by Sri Trang Gloves (Thailand) Public Company Limited (Hatyai, TH). The FDA issued a Cleared decision on March 20, 2020, 88 days after receiving the submission on December 23, 2019. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.6250.
| 510(k) Number | K193581 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | December 23, 2019 |
| Decision Date | March 20, 2020 |
| Days to Decision | 88 days |
| Submission Type | Abbreviated |
| 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. |