Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NON-INVASIVE BLOOD PRESSURE MODULE

K-Number: K875265 · 1988-02-29

ApplicantPpg Industries, Inc.
Decision Date1988-02-29
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NON-INVASIVE BLOOD PRESSURE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Ppg Industries, Inc.. It received FDA 510(k) clearance on 1988-02-29 under 510(k) number K875265. 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 NON-INVASIVE BLOOD PRESSURE MODULE?

NON-INVASIVE BLOOD PRESSURE MODULE is a medical device that received FDA 510(k) clearance on 1988-02-29. The listed applicant is Ppg Industries, Inc.. The 510(k) number is K875265.

When did NON-INVASIVE BLOOD PRESSURE MODULE receive FDA 510(k) clearance?

NON-INVASIVE BLOOD PRESSURE MODULE received FDA 510(k) clearance on 1988-02-29, under 510(k) number K875265.

Who is the listed applicant for NON-INVASIVE BLOOD PRESSURE MODULE?

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

What is the FDA product code for NON-INVASIVE BLOOD PRESSURE MODULE?

The FDA product code for NON-INVASIVE BLOOD PRESSURE MODULE is DXN.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ppg Industries, 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.

K922631STATPAL II BLOOD GAS ANALYSIS SYSTEMK913358MIDAS SYSTEM(TM) 5100 PHYSIOLOG MONIT/RECORD SYSTK914560STAT PAL SENSYR SYRINGE ASSEMBLY FOR USE W/STATPALK912627MIDAS SYSTEM 2500, PHYSIOLOGICAL MONITORING SYSTEMK903965STATPAL BLOOD GAS MONITORING SYSTEMK901514XR MODEL H PHYSIOLOGICAL MONITOR & RECORDING SYS.

View all 20 devices →

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.

↑