The following data is part of a premarket notification filed by Hti Trading Group with the FDA for Baldur Latex Examination Gloves.
Device ID | K923707 |
510k Number | K923707 |
Device Name: | BALDUR LATEX EXAMINATION GLOVES |
Classification | Latex Patient Examination Glove |
Applicant | HTI TRADING GROUP 3423 INVESTMENT BLVD. SUITE 12 Hayward, CA 94545 |
Contact | David Hu |
Correspondent | David Hu HTI TRADING GROUP 3423 INVESTMENT BLVD. SUITE 12 Hayward, CA 94545 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-27 |
Decision Date | 1992-11-17 |