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FDA 510(k)

MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY

K-Number: K042273 · 2004-08-31

ApplicantHealth Hero Network, Inc.
Decision Date2004-08-31
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY is the device name listed in this FDA 510(k) record. The listed applicant is Health Hero Network, Inc.. It received FDA 510(k) clearance on 2004-08-31 under 510(k) number K042273. 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 MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY?

MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY is a medical device that received FDA 510(k) clearance on 2004-08-31. The listed applicant is Health Hero Network, Inc.. The 510(k) number is K042273.

When did MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY receive FDA 510(k) clearance?

MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY received FDA 510(k) clearance on 2004-08-31, under 510(k) number K042273.

Who is the listed applicant for MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY?

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

What is the FDA product code for MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY?

The FDA product code for MODIFICATION TO HEALTH BUDDY WITH DEVICE CONNECTIVITY is DXN.

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Other records listing Health Hero Network, 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.

K080091MODIFICATION TO:HEALTH BUDDY APPLIANCEK070543MODIFICATION TO HEALTH BUDDY APPLIANCEK063612MODIFICATION TO HEALTH BUDDY APPLIANCEK060843MODIFICATION TO HEALTH BUDDY APPLIANCEK050567HEALTH BUDDY APPLIANCEK040086HEALTH BUDDY WITH BUDDYLINK

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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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