The following data is part of a premarket notification filed by Alan S. Lee with the FDA for Ms-700.
| Device ID | K972213 |
| 510k Number | K972213 |
| Device Name: | MS-700 |
| Classification | Flowmeter, Blood, Cardiovascular |
| Applicant | ALAN S. LEE 2121 W BEACON AVE. Anaheim, CA 92804 |
| Contact | Alan S Lee |
| Correspondent | Alan S Lee ALAN S. LEE 2121 W BEACON AVE. Anaheim, CA 92804 |
| Product Code | DPW |
| CFR Regulation Number | 870.2100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-12 |
| Decision Date | 1998-03-13 |
| Summary: | summary |