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)

PLETHYSMOGRAPH (MDI SYSTEM II)

K-Number: K760504 · 1976-08-26

ApplicantMarketing Development Intl.
Decision Date1976-08-26
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PLETHYSMOGRAPH (MDI SYSTEM II) is the device name listed in this FDA 510(k) record. The listed applicant is Marketing Development Intl.. It received FDA 510(k) clearance on 1976-08-26 under 510(k) number K760504. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLETHYSMOGRAPH (MDI SYSTEM II)?

PLETHYSMOGRAPH (MDI SYSTEM II) is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is Marketing Development Intl.. The 510(k) number is K760504.

When did PLETHYSMOGRAPH (MDI SYSTEM II) receive FDA 510(k) clearance?

PLETHYSMOGRAPH (MDI SYSTEM II) received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760504.

Who is the listed applicant for PLETHYSMOGRAPH (MDI SYSTEM II)?

The FDA 510(k) record lists Marketing Development Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLETHYSMOGRAPH (MDI SYSTEM II)?

The FDA product code for PLETHYSMOGRAPH (MDI SYSTEM II) is JOM.

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

Related Devices (Code: JOM)

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.

K220527PADnet XpressCollaborative Care Diagnostics, LLC, D.B.A. BiomedixK213730MESI mTABLET TBI diagnostic system, MESI mTABLET TBIMesi, Development of Medical Devices, Ltd.; Mesi D.O.O.K200567ASI Plethysmogrpah AnalyzerArterial Stiffness, Inc.K201046Automated ankle brachial pressure index measuring device, MESI mTABLET systemMesi D.O.O.; Mesi, Development of Medical Devices, Ltd.K191266VitalScan ANSMedeia, Inc.K172655Automated ankle brachial pressure index measuring deviceMesi D.O.O.; Mesi, Development of Medical Devices, Ltd.

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.

↑