The following data is part of a premarket notification filed by Pt. Irama Dinamika Latex with the FDA for Hypoallergenic Latex Patient Exam Gloves-prepowdered.
Device ID | K980848 |
510k Number | K980848 |
Device Name: | HYPOALLERGENIC LATEX PATIENT EXAM GLOVES-PREPOWDERED |
Classification | Latex Patient Examination Glove |
Applicant | PT. IRAMA DINAMIKA LATEX JL. KAPTEN PATTIMURA NO. 23/ 235 MEDAN 21053 Indonesia, ID |
Contact | Anil Taneja |
Correspondent | Anil Taneja PT. IRAMA DINAMIKA LATEX JL. KAPTEN PATTIMURA NO. 23/ 235 MEDAN 21053 Indonesia, ID |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-03-04 |
Decision Date | 1998-04-28 |