The following data is part of a premarket notification filed by Smart Glove Corp. Sdn Bhd with the FDA for Nitrile Pre-powdered Examination Gloves.
| Device ID | K974907 |
| 510k Number | K974907 |
| Device Name: | NITRILE PRE-POWDERED EXAMINATION GLOVES |
| Classification | Polymer Patient Examination Glove |
| Applicant | SMART GLOVE CORP. SDN BHD BATU 5 3/4, JALAN KAPAR KLANG Selangor Darul Eshan, MY 42100 |
| Contact | Foo K Pu |
| Correspondent | Foo K Pu SMART GLOVE CORP. SDN BHD BATU 5 3/4, JALAN KAPAR KLANG Selangor Darul Eshan, MY 42100 |
| Product Code | LZA |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-12-31 |
| Decision Date | 1998-03-13 |