The following data is part of a premarket notification filed by Wembley Rubber Products (m) Sdn Bhd with the FDA for Comfit, Patient Examination Gloves.
Device ID | K903746 |
510k Number | K903746 |
Device Name: | COMFIT, PATIENT EXAMINATION GLOVES |
Classification | Patient Examination Glove |
Applicant | WEMBLEY RUBBER PRODUCTS (M) SDN BHD 11TH FLOOR, MENARA APERA ULG 84, JALAN RAJA CHULAN 50200 Kuala Lumpur, Malaysia, MY |
Contact | Eng Keat |
Correspondent | Eng Keat WEMBLEY RUBBER PRODUCTS (M) SDN BHD 11TH FLOOR, MENARA APERA ULG 84, JALAN RAJA CHULAN 50200 Kuala Lumpur, Malaysia, MY |
Product Code | FMC |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-08-13 |
Decision Date | 1990-09-05 |