The following data is part of a premarket notification filed by Astro-med, Inc. with the FDA for Mt9000 Chart Recorder.
| Device ID | K892067 |
| 510k Number | K892067 |
| Device Name: | MT9000 CHART RECORDER |
| Classification | Recorder, Magnetic Tape, Medical |
| Applicant | ASTRO-MED, INC. 600 EAST GREENWICH AVE. West Warwick, RI 02893 |
| Contact | Donna J Ray |
| Correspondent | Donna J Ray ASTRO-MED, INC. 600 EAST GREENWICH AVE. West Warwick, RI 02893 |
| Product Code | DSH |
| CFR Regulation Number | 870.2800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-03-30 |
| Decision Date | 1989-06-05 |