The following data is part of a premarket notification filed by Integrated Display Technology, Ltd. with the FDA for Integrated Display Technology Ltd..
| Device ID | K853130 |
| 510k Number | K853130 |
| Device Name: | INTEGRATED DISPLAY TECHNOLOGY LTD. |
| Classification | Thermometer, Electronic, Clinical |
| Applicant | INTEGRATED DISPLAY TECHNOLOGY, LTD. 41, MAN YUE ST., KAISER ESTATE BLOCK C, 9/F, HUNG HOM, Kowloon, Hong Kong, HK |
| Contact | Shirley Chan |
| Correspondent | Shirley Chan INTEGRATED DISPLAY TECHNOLOGY, LTD. 41, MAN YUE ST., KAISER ESTATE BLOCK C, 9/F, HUNG HOM, Kowloon, Hong Kong, HK |
| Product Code | FLL |
| CFR Regulation Number | 880.2910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-07-26 |
| Decision Date | 1985-11-08 |