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FDA 510(k)

CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI

K-Number: K924530 · 1993-02-05

ApplicantCabot Medical Corp.
Decision Date1993-02-05
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI 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 1993-02-05 under 510(k) number K924530. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI?

CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is Cabot Medical Corp.. The 510(k) number is K924530.

When did CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI receive FDA 510(k) clearance?

CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI received FDA 510(k) clearance on 1993-02-05, under 510(k) number K924530.

Who is the listed applicant for CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI?

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(TM) 3.0 LITER HIGH FLOW IRRI?

The FDA product code for CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI is HET.

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Other records listing Cabot Medical Corp. as applicant

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Related Devices (Code: HET)

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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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