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FDA 510(k)

CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP

K-Number: K941743 · 1995-04-19

ApplicantCabot Medical Corp.
Decision Date1995-04-19
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1995-04-19 under 510(k) number K941743. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP?

CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP is a medical device that received FDA 510(k) clearance on 1995-04-19. The listed applicant is Cabot Medical Corp.. The 510(k) number is K941743.

When did CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP receive FDA 510(k) clearance?

CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP received FDA 510(k) clearance on 1995-04-19, under 510(k) number K941743.

Who is the listed applicant for CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP?

The FDA 510(k) record lists Cabot Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP?

The FDA product code for CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP is HIG.

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Other records listing Cabot Medical Corp. 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.

K960148CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENTK946109CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPSK951972CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHSK951714CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBERK9341153000 ELECTRONIC INSUFFLATOR MODIFICATIONK932293CABOT MEDICAL BIPOLAR CUTTING FORCEPS

View all 38 devices →

Related Devices (Code: HIG)

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.

K261706Endomat Select (UP220)KARL STORZ SE & CO. KGK251273Asurys Fluid Management SystemBoston Scientific CorporationK240886Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205)Hologic, Inc.K210628X-FLO Fluid Management SystemThermedx, LLCK201355Endomat Select, IBS Shaver Software, LicenseKarl Storz SE & CO. KGK180735Endomat SelectKarl Storz SE & CO. KG

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.

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