The following data is part of a premarket notification filed by Cypress Medical Products, Ltd. with the FDA for Cypress Medical Products Aneroid Sphygmomanometer.
| Device ID | K972899 |
| 510k Number | K972899 |
| Device Name: | CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETER |
| Classification | Blood Pressure Cuff |
| Applicant | CYPRESS MEDICAL PRODUCTS, LTD. 1202 SOUTH ROUTE 31 Mchenry, IL 60050 |
| Contact | Anthony L Giaccio |
| Correspondent | Anthony L Giaccio CYPRESS MEDICAL PRODUCTS, LTD. 1202 SOUTH ROUTE 31 Mchenry, IL 60050 |
| Product Code | DXQ |
| CFR Regulation Number | 870.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-06 |
| Decision Date | 1998-07-07 |