The following data is part of a premarket notification filed by Copioumed Intl., Inc. with the FDA for Poly (vinyl) Exam Glove, Powder-free.
Device ID | K972624 |
510k Number | K972624 |
Device Name: | POLY (VINYL) EXAM GLOVE, POWDER-FREE |
Classification | Vinyl Patient Examination Glove |
Applicant | COPIOUMED INTL., INC. 19001 S. RICHFIELD #185 Green Valley, AZ 85614 |
Contact | Janna P Tucker |
Correspondent | Janna P Tucker COPIOUMED INTL., INC. 19001 S. RICHFIELD #185 Green Valley, AZ 85614 |
Product Code | LYZ |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-07-14 |
Decision Date | 1997-11-06 |