The following data is part of a premarket notification filed by P.t. Latexindo Tobaperkasa with the FDA for Hi Coat.
| Device ID | K972539 |
| 510k Number | K972539 |
| Device Name: | HI COAT |
| Classification | Latex Patient Examination Glove |
| Applicant | P.T. LATEXINDO TOBAPERKASA JALAN RAYA BINJAI KM. 11. Medan, ID |
| Contact | Hendra Ramali |
| Correspondent | Hendra Ramali P.T. LATEXINDO TOBAPERKASA JALAN RAYA BINJAI KM. 11. Medan, ID |
| Product Code | LYY |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-07-08 |
| Decision Date | 1997-11-18 |