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)

ADJUSTABLE BALLOON DISSECTION CANNULA

K-Number: K940875 · 1994-05-03

ApplicantOrigin Medsystems, Inc.
Decision Date1994-05-03
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADJUSTABLE BALLOON DISSECTION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1994-05-03 under 510(k) number K940875. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADJUSTABLE BALLOON DISSECTION CANNULA?

ADJUSTABLE BALLOON DISSECTION CANNULA is a medical device that received FDA 510(k) clearance on 1994-05-03. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K940875.

When did ADJUSTABLE BALLOON DISSECTION CANNULA receive FDA 510(k) clearance?

ADJUSTABLE BALLOON DISSECTION CANNULA received FDA 510(k) clearance on 1994-05-03, under 510(k) number K940875.

Who is the listed applicant for ADJUSTABLE BALLOON DISSECTION CANNULA?

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

What is the FDA product code for ADJUSTABLE BALLOON DISSECTION CANNULA?

The FDA product code for ADJUSTABLE BALLOON DISSECTION CANNULA is GCJ.

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 Origin Medsystems, 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.

K992353BLUNT TIP TROCAR PORTK981700VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEMK972685ORIGIN LIGATOR DEVICEK970611ORIGIN CARDIAC STABLIZER OCCLUDERK965121CANNULAK964171VASOVIEW BALLOON DISSECTION SYSTEM

View all 50 devices →

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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.

↑