The following data is part of a premarket notification filed by Oon Corp. Resources with the FDA for Patient Examination Gloves (latex).
| Device ID | K891511 |
| 510k Number | K891511 |
| Device Name: | PATIENT EXAMINATION GLOVES (LATEX) |
| Classification | Latex Patient Examination Glove |
| Applicant | OON CORP. RESOURCES NO. 59, SENAWANG INDUST ESTATE 70450 SEREMBAN, NEGERI Sembilan, Malaysia, MY |
| Contact | Koh Oon |
| Correspondent | Koh Oon OON CORP. RESOURCES NO. 59, SENAWANG INDUST ESTATE 70450 SEREMBAN, NEGERI Sembilan, Malaysia, MY |
| Product Code | LYY |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-03-16 |
| Decision Date | 1989-03-29 |