ANEROID TYPE BLOOD PRESSURE KIT

Blood Pressure Cuff

MARS METAL CO., LTD.

The following data is part of a premarket notification filed by Mars Metal Co., Ltd. with the FDA for Aneroid Type Blood Pressure Kit.

Pre-market Notification Details

Device IDK780715
510k NumberK780715
Device Name:ANEROID TYPE BLOOD PRESSURE KIT
ClassificationBlood Pressure Cuff
Applicant MARS METAL CO., LTD. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeDXQ  
CFR Regulation Number870.1120 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-04-27
Decision Date1978-07-17

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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

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