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)

MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR

K-Number: K912750 · 1991-08-02

ApplicantDexide, Inc.
Decision Date1991-08-02
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1991-08-02 under 510(k) number K912750. 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 MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR?

MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR is a medical device that received FDA 510(k) clearance on 1991-08-02. The listed applicant is Dexide, Inc.. The 510(k) number is K912750.

When did MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR receive FDA 510(k) clearance?

MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR received FDA 510(k) clearance on 1991-08-02, under 510(k) number K912750.

Who is the listed applicant for MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR?

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

What is the FDA product code for MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR?

The FDA product code for MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR 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 Dexide, 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.

K991814MULTACHOICE INSTRUMENTSK990379MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIESK981940MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIESK981941MULTAPORT CANNULA REDUCER AND ACCESSORIESK953611DEXIDE ENDO-LUBE KITK944509DEXIDE INSUFFLATION TUBING WITH FILTER

View all 38 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.

↑