The following data is part of a premarket notification filed by Pamitex Industries Sdn Bhd with the FDA for Health-plus, Sanitex, Reliance Pre-powdered Nitrile Examination Glove.
| Device ID | K992299 |
| 510k Number | K992299 |
| Device Name: | HEALTH-PLUS, SANITEX, RELIANCE PRE-POWDERED NITRILE EXAMINATION GLOVE |
| Classification | Polymer Patient Examination Glove |
| Applicant | PAMITEX INDUSTRIES SDN BHD 2 1/2 MILES, JALAN RASAH SEREMBAN, NAGERI SEMBILAN Darul Khusus, MY 70300 |
| Contact | Said Awang |
| Correspondent | Said Awang PAMITEX INDUSTRIES SDN BHD 2 1/2 MILES, JALAN RASAH SEREMBAN, NAGERI SEMBILAN Darul Khusus, MY 70300 |
| Product Code | LZA |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-08 |
| Decision Date | 1999-08-23 |