The following data is part of a premarket notification filed by Pm Gloves, Inc. with the FDA for Pm Gloves (mfg: Bjl Glove (m) Sdn.bhd.).
Device ID | K902670 |
510k Number | K902670 |
Device Name: | PM GLOVES (MFG: BJL GLOVE (M) SDN.BHD.) |
Classification | Latex Patient Examination Glove |
Applicant | PM GLOVES, INC. 14145 PROCTOR AVE. SUITE #21 City Of Industry, CA 91746 |
Contact | Andy K Lin |
Correspondent | Andy K Lin PM GLOVES, INC. 14145 PROCTOR AVE. SUITE #21 City Of Industry, CA 91746 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-06-18 |
Decision Date | 1990-09-05 |