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FDA 510(k)

MODIFICATION TO: BPCARD, MODEL Z-7000-0700

K-Number: K073630 · 2008-01-11

ApplicantQrs Diagnostic, LLC
Decision Date2008-01-11
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: BPCARD, MODEL Z-7000-0700 is the device name listed in this FDA 510(k) record. The listed applicant is Qrs Diagnostic, LLC. It received FDA 510(k) clearance on 2008-01-11 under 510(k) number K073630. 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: BPCARD, MODEL Z-7000-0700?

MODIFICATION TO: BPCARD, MODEL Z-7000-0700 is a medical device that received FDA 510(k) clearance on 2008-01-11. The listed applicant is Qrs Diagnostic, LLC. The 510(k) number is K073630.

When did MODIFICATION TO: BPCARD, MODEL Z-7000-0700 receive FDA 510(k) clearance?

MODIFICATION TO: BPCARD, MODEL Z-7000-0700 received FDA 510(k) clearance on 2008-01-11, under 510(k) number K073630.

Who is the listed applicant for MODIFICATION TO: BPCARD, MODEL Z-7000-0700?

The FDA 510(k) record lists Qrs Diagnostic, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO: BPCARD, MODEL Z-7000-0700?

The FDA product code for MODIFICATION TO: BPCARD, MODEL Z-7000-0700 is DXN.

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Other records listing Qrs Diagnostic, LLC 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.

K083749CARDIOVIEW32 REVIEW MODULEK031964BPCARDK030535EKGCARD SYSTEMK001278SENSAIRE DIAGNOSTIC SPIROMETERK001995SPIROXCARD DIAGNOSTIC SPIROMETER AND PULSE OXIMETERK973138SPIROCARD

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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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