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FDA 510(k)

DIGITAL SPHYGMOMANOMETER MODEL 7620

K-Number: K853158 · 1985-11-14

ApplicantTakeda Medical, Inc.
Decision Date1985-11-14
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL SPHYGMOMANOMETER MODEL 7620 is the device name listed in this FDA 510(k) record. The listed applicant is Takeda Medical, Inc.. It received FDA 510(k) clearance on 1985-11-14 under 510(k) number K853158. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL SPHYGMOMANOMETER MODEL 7620?

DIGITAL SPHYGMOMANOMETER MODEL 7620 is a medical device that received FDA 510(k) clearance on 1985-11-14. The listed applicant is Takeda Medical, Inc.. The 510(k) number is K853158.

When did DIGITAL SPHYGMOMANOMETER MODEL 7620 receive FDA 510(k) clearance?

DIGITAL SPHYGMOMANOMETER MODEL 7620 received FDA 510(k) clearance on 1985-11-14, under 510(k) number K853158.

Who is the listed applicant for DIGITAL SPHYGMOMANOMETER MODEL 7620?

The FDA 510(k) record lists Takeda Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL SPHYGMOMANOMETER MODEL 7620?

The FDA product code for DIGITAL SPHYGMOMANOMETER MODEL 7620 is DXN.

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Other records listing Takeda Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K854797TAKEDA MEDICAL DIGITAL SPHYGMOMANOMETER, UA-731K851223COPAL DIGITAL SPHYGMOMANOMETER UA-560K852564COPAL UA-512 DIGITAL BLOOD PRESSURE MONITORK843390COPAL DIGITAL SPHYGMOMANOMETER UA-535K844285COPAL DIGITAL SPHYGMOMAMOMETER UA-550K842388COPAL DIGITAL SPHYGMOMANOMETER UA-510

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Related Devices (Code: DXN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261929Upper Arm Blood pressure monitor (BP7155D)OMRON Healthcare, Inc.K254000Happy Health Blood Pressure MonitorHappy Health, Inc.K262658Automatic Digital Blood Pressure monitor (LD-526)Honsun (Nantong) Co., Ltd.K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus, DBP-61E3 Plus, DBP-61E2 Plus, DBP-62E3B Plus, DBP-62E2B Plus)JOYTECH Healthcare Co., Ltd.K253425Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)Joytech Healthcare Co. , Ltd.K261061BP Go (BPP-855)Wellvii, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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