The following data is part of a premarket notification filed by Shimadzu Medical Systems with the FDA for Shimadzu Image Amplifier Ia-12lm Series.
| Device ID | K936236 |
| 510k Number | K936236 |
| Device Name: | SHIMADZU IMAGE AMPLIFIER IA-12LM SERIES |
| Classification | System, X-ray, Fluoroscopic, Image-intensified |
| Applicant | SHIMADZU MEDICAL SYSTEMS 20101 SOUTH VERMONT AVE. Torrance, CA 90502 -1328 |
| Contact | Michael Y Fishback |
| Correspondent | Michael Y Fishback SHIMADZU MEDICAL SYSTEMS 20101 SOUTH VERMONT AVE. Torrance, CA 90502 -1328 |
| Product Code | JAA |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-12-30 |
| Decision Date | 1995-05-11 |