The following data is part of a premarket notification filed by Glormed Intl., Inc. with the FDA for Vinyl Exam Gloves, Powder Free.
Device ID | K983494 |
510k Number | K983494 |
Device Name: | VINYL EXAM GLOVES, POWDER FREE |
Classification | Vinyl Patient Examination Glove |
Applicant | GLORMED INTL., INC. 198 AVENUE DE LA D'EMERALD Sparks, NV 89434 |
Contact | Janna P Tucker |
Correspondent | Janna P Tucker GLORMED INTL., INC. 198 AVENUE DE LA D'EMERALD Sparks, NV 89434 |
Product Code | LYZ |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-10-05 |
Decision Date | 1998-11-05 |
Summary: | summary |