The following data is part of a premarket notification filed by Shun Thai Rubber Gloves Industry Co., Ltd. with the FDA for Hypo-allergenic Patient Examination Gloves.
Device ID | K930139 |
510k Number | K930139 |
Device Name: | HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES |
Classification | Latex Patient Examination Glove |
Applicant | SHUN THAI RUBBER GLOVES INDUSTRY CO., LTD. 238/1 RATCHADA-PISEK ROAD HUAY-KWANG, BANGKOK 10310 Thailand, TH |
Contact | Khun T Surangkana |
Correspondent | Khun T Surangkana SHUN THAI RUBBER GLOVES INDUSTRY CO., LTD. 238/1 RATCHADA-PISEK ROAD HUAY-KWANG, BANGKOK 10310 Thailand, TH |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-01-12 |
Decision Date | 1993-08-24 |