The following data is part of a premarket notification filed by Pt. Irama Dinamika Latex with the FDA for Flavored Latex Patient Examination.
| Device ID | K960315 |
| 510k Number | K960315 |
| Device Name: | FLAVORED LATEX PATIENT EXAMINATION |
| 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 | 1996-01-23 |
| Decision Date | 1996-11-20 |