The following data is part of a premarket notification filed by Wembley Rubber Products (m) Sdn Bhd with the FDA for Comfit (sterile).
| Device ID | K944141 |
| 510k Number | K944141 |
| Device Name: | COMFIT (STERILE) |
| Classification | Latex Patient Examination Glove |
| Applicant | WEMBLEY RUBBER PRODUCTS (M) SDN BHD KAWASAN PERUSAHAAN BANDAR BARU LOT 1, JALAN 3 Sepang Selangor, MY 43900 |
| Contact | Ong Ghee Chee |
| Correspondent | Ong Ghee Chee WEMBLEY RUBBER PRODUCTS (M) SDN BHD KAWASAN PERUSAHAAN BANDAR BARU LOT 1, JALAN 3 Sepang Selangor, MY 43900 |
| Product Code | LYY |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-25 |
| Decision Date | 1994-10-13 |