The following data is part of a premarket notification filed by Jenq Chuam Industrial Co., Ltd. with the FDA for Patient Examination Gloves (latex).
Device ID | K892103 |
510k Number | K892103 |
Device Name: | PATIENT EXAMINATION GLOVES (LATEX) |
Classification | Latex Patient Examination Glove |
Applicant | JENQ CHUAM INDUSTRIAL CO., LTD. NO. 837-1, CHUNG HO ST. HSIN SEH SHIANG Taichung Hsien, Taiwan, TW |
Contact | Lian-chi Jan |
Correspondent | Lian-chi Jan JENQ CHUAM INDUSTRIAL CO., LTD. NO. 837-1, CHUNG HO ST. HSIN SEH SHIANG Taichung Hsien, Taiwan, TW |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-04-03 |
Decision Date | 1989-05-22 |