The following data is part of a premarket notification filed by Thai Nam Rubber Gloves Co., Ltd. with the FDA for Patient Examination Gloves (latex).
Device ID | K891702 |
510k Number | K891702 |
Device Name: | PATIENT EXAMINATION GLOVES (LATEX) |
Classification | Latex Patient Examination Glove |
Applicant | THAI NAM RUBBER GLOVES CO., LTD. 3710 W. MONTROSE AVE. Chicago, IL 60618 |
Contact | Lee Bingham |
Correspondent | Lee Bingham THAI NAM RUBBER GLOVES CO., LTD. 3710 W. MONTROSE AVE. Chicago, IL 60618 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-03-20 |
Decision Date | 1989-06-19 |