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 |