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)

MOTILITY MEASUREMENT SYS MMS-100

K-Number: K832869 · 1983-10-31

ApplicantNarco Bio-Systems
Decision Date1983-10-31
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOTILITY MEASUREMENT SYS MMS-100 is the device name listed in this FDA 510(k) record. The listed applicant is Narco Bio-Systems. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K832869. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTILITY MEASUREMENT SYS MMS-100?

MOTILITY MEASUREMENT SYS MMS-100 is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Narco Bio-Systems. The 510(k) number is K832869.

When did MOTILITY MEASUREMENT SYS MMS-100 receive FDA 510(k) clearance?

MOTILITY MEASUREMENT SYS MMS-100 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832869.

Who is the listed applicant for MOTILITY MEASUREMENT SYS MMS-100?

The FDA 510(k) record lists Narco Bio-Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOTILITY MEASUREMENT SYS MMS-100?

The FDA product code for MOTILITY MEASUREMENT SYS MMS-100 is FFX.

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 Narco Bio-Systems 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.

K853683UMS-100K833656NARCOTRACE 40 - NT40K813502NARCO TELECARE ISOFLO PRESSURE MONITORK811376ULTRASONIC QFM SYSTEM 1000K810431NARCO TLECARE MINIATURE PRESSURE DOMEK801544PORTA-FIB LPD

View all 9 devices →

Related Devices (Code: FFX)

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.

K252605mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001)Medspira, LLCK240007Solar Compact (G4-1)Laborie Medical Technologies, Corp.K231861EndoflipTM 300 SystemCovidien, LLCK223705EndoflipTM 300Covidien, LLCK222000Transit-PelletsMedifactia ABK201106IntraMarX 3D Radiopaque MarkerAnx Robotica Corp

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.

↑