The following data is part of a premarket notification filed by Fitco Dipped Products Pvt. Ltd with the FDA for Sterile Latex Powdered Patient Examination Gloves.
Device ID | K000891 |
510k Number | K000891 |
Device Name: | STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES |
Classification | Latex Patient Examination Glove |
Applicant | FITCO DIPPED PRODUCTS PVT. LTD 14-A COCHIN EXPORT PROCESSING ZONE, KAKKANAND, KOCHIN Kerala, IN 682 030 |
Contact | Joseph J E Pereira |
Correspondent | Joseph J E Pereira FITCO DIPPED PRODUCTS PVT. LTD 14-A COCHIN EXPORT PROCESSING ZONE, KAKKANAND, KOCHIN Kerala, IN 682 030 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-03-20 |
Decision Date | 2000-04-28 |