The following data is part of a premarket notification filed by Hti Trading Group with the FDA for Baldur Latex Examination Gloves.
Device ID | K902644 |
510k Number | K902644 |
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 Ju |
Correspondent | David Ju 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 | 1990-06-15 |
Decision Date | 1990-07-11 |