The following data is part of a premarket notification filed by Mars Metal Co., Ltd. with the FDA for Aneroid Type Blood Pressure Kit.
| Device ID | K780715 |
| 510k Number | K780715 |
| Device Name: | ANEROID TYPE BLOOD PRESSURE KIT |
| Classification | Blood Pressure Cuff |
| Applicant | MARS METAL CO., LTD. 803 N. Front St. Suite 3 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 | 1978-04-27 |
| Decision Date | 1978-07-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20665973017079 | K780715 | 000 |
| 00073796010409 | K780715 | 000 |
| 00073796010423 | K780715 | 000 |
| 00073796112004 | K780715 | 000 |
| 20665973016874 | K780715 | 000 |
| 20665973016881 | K780715 | 000 |
| 20665973016898 | K780715 | 000 |
| 20665973016904 | K780715 | 000 |
| 20665973016911 | K780715 | 000 |
| 20665973016966 | K780715 | 000 |
| 20665973016973 | K780715 | 000 |
| 20665973016980 | K780715 | 000 |
| 20665973016997 | K780715 | 000 |
| 20665973017000 | K780715 | 000 |
| 20665973017062 | K780715 | 000 |
| 00073796000189 | K780715 | 000 |