The following data is part of a premarket notification filed by Northstar Healthcare Holdings with the FDA for Utb Blue Powder Free Nitrile.
Device ID | K121506 |
510k Number | K121506 |
Device Name: | UTB BLUE POWDER FREE NITRILE |
Classification | Polymer Patient Examination Glove |
Applicant | NORTHSTAR HEALTHCARE HOLDINGS HAMILTON HOUSE, 10 QUEEN ST Hamilton, Bermuda, IE Hm11 |
Contact | Wesley Toavs |
Correspondent | Ned Devine UNDERWRITERS LABORATORIES, INC. 333 PFINGSTEN RD. Northbrook, IL 60062 |
Product Code | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2012-05-21 |
Decision Date | 2012-07-03 |
Summary: | summary |