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FDA 510(k)

DINAMAP MODEL 835

K-Number: K771896 · 1977-10-25

ApplicantApplied Medical Research
Decision Date1977-10-25
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DINAMAP MODEL 835 is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Research. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771896. 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 DINAMAP MODEL 835?

DINAMAP MODEL 835 is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Applied Medical Research. The 510(k) number is K771896.

When did DINAMAP MODEL 835 receive FDA 510(k) clearance?

DINAMAP MODEL 835 received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771896.

Who is the listed applicant for DINAMAP MODEL 835?

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

What is the FDA product code for DINAMAP MODEL 835?

The FDA product code for DINAMAP MODEL 835 is DXN.

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Other records listing Applied Medical Research 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.

K800025DINAMAP RESEARCH MONITOR 1245K791580CEREBRAL FUNCTION MONITOR 870K791159DINAMAP MODEL 855K790322OPTIONAL ACCESSORY FOOT SWITCH MODEL 100K790328MODEL 1051, MONITORK782073DINAMAP MODELS 1160 AND 1165

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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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