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)

HEAT AND MOISTURE EXCHANGERS AND FILTERS

K-Number: K941987 · 1994-08-15

ApplicantIcor AB
Decision Date1994-08-15
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HEAT AND MOISTURE EXCHANGERS AND FILTERS is the device name listed in this FDA 510(k) record. The listed applicant is Icor AB. It received FDA 510(k) clearance on 1994-08-15 under 510(k) number K941987. The device is classified under product code BYD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEAT AND MOISTURE EXCHANGERS AND FILTERS?

HEAT AND MOISTURE EXCHANGERS AND FILTERS is a medical device that received FDA 510(k) clearance on 1994-08-15. The listed applicant is Icor AB. The 510(k) number is K941987.

When did HEAT AND MOISTURE EXCHANGERS AND FILTERS receive FDA 510(k) clearance?

HEAT AND MOISTURE EXCHANGERS AND FILTERS received FDA 510(k) clearance on 1994-08-15, under 510(k) number K941987.

Who is the listed applicant for HEAT AND MOISTURE EXCHANGERS AND FILTERS?

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 HEAT AND MOISTURE EXCHANGERS AND FILTERS?

The FDA product code for HEAT AND MOISTURE EXCHANGERS AND FILTERS is BYD.

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.

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.

View all 16 devices →

Related Devices (Code: BYD)

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.

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.

↑