The following data is part of a premarket notification filed by Pt. Irama Dinamika Latex with the FDA for Patient Examination Gloves.
Device ID | K953462 |
510k Number | K953462 |
Device Name: | PATIENT EXAMINATION GLOVES |
Classification | Latex Patient Examination Glove |
Applicant | PT. IRAMA DINAMIKA LATEX JL. KAPTEN PATTIMURA NO. Medan, ID 20153 |
Contact | Anil Taneja |
Correspondent | Anil Taneja PT. IRAMA DINAMIKA LATEX JL. KAPTEN PATTIMURA NO. Medan, ID 20153 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-07-24 |
Decision Date | 1996-01-04 |