The following data is part of a premarket notification filed by Perusahaan Getah Asas Sdn Bhd with the FDA for Nitrile Patient Examination Glove.
Device ID | K982440 |
510k Number | K982440 |
Device Name: | NITRILE PATIENT EXAMINATION GLOVE |
Classification | Polymer Patient Examination Glove |
Applicant | PERUSAHAAN GETAH ASAS SDN BHD LOT 754, JALAN HAJI SIRAT OFF JALAN KAPAR, KLANG Selangor, Darul Ehsan, MY 42100 |
Contact | Bob Chan |
Correspondent | Bob Chan PERUSAHAAN GETAH ASAS SDN BHD LOT 754, JALAN HAJI SIRAT OFF JALAN KAPAR, KLANG Selangor, Darul Ehsan, 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 | 1998-07-14 |
Decision Date | 1998-09-30 |