The following data is part of a premarket notification filed by Ansell Healthcare Products Llc with the FDA for Micro-touch Nitrafree.
Device ID | K080536 |
510k Number | K080536 |
Device Name: | MICRO-TOUCH NITRAFREE |
Classification | Polymer Patient Examination Glove |
Applicant | ANSELL HEALTHCARE PRODUCTS LLC 1635 INDUSTRIAL RD. Dothan, AL 36303 |
Contact | Lon D Mciivain |
Correspondent | Lon D Mciivain ANSELL HEALTHCARE PRODUCTS LLC 1635 INDUSTRIAL RD. Dothan, AL 36303 |
Product Code | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-02-27 |
Decision Date | 2008-06-19 |
Summary: | summary |