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FDA 510(k)

ICOR CMU Q PLUS

K-Number: K895935 · 1990-01-04

ApplicantIcor AB
Decision Date1990-01-04
Product CodeBZL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ICOR CMU Q PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Icor AB. It received FDA 510(k) clearance on 1990-01-04 under 510(k) number K895935. The device is classified under product code BZL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ICOR CMU Q PLUS?

ICOR CMU Q PLUS is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is Icor AB. The 510(k) number is K895935.

When did ICOR CMU Q PLUS receive FDA 510(k) clearance?

ICOR CMU Q PLUS received FDA 510(k) clearance on 1990-01-04, under 510(k) number K895935.

Who is the listed applicant for ICOR CMU Q PLUS?

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

What is the FDA product code for ICOR CMU Q PLUS?

The FDA product code for ICOR CMU Q PLUS is BZL.

Other records listing Icor AB 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.

K954402ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)K953507TYPE 1 & 2 (HUMIDAIR I & II)K952325ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)K952823FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBEK941987HEAT AND MOISTURE EXCHANGERS AND FILTERSK940041COLIBRI

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Related Devices (Code: BZL)

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.

K200076Breezing MedTf Health Co.K190561NICU V'02Cosmed Nordic ApsK110810ANASCIENT BREATH MONITORInvoy Technologies, LLCK093080METAPHOR METABOLIC MONITORTreymed, Inc.K071533FITMATE SERIESCosmed SrlK070858EXPRESS SERIESMedical Graphics 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.

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