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)

INTERTECH(TM) HEAT AND MOISTURE EXCHANGER

K-Number: K903519 · 1990-12-13

ApplicantIntertech Resources, Inc.
Decision Date1990-12-13
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTERTECH(TM) HEAT AND MOISTURE EXCHANGER is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1990-12-13 under 510(k) number K903519. 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 INTERTECH(TM) HEAT AND MOISTURE EXCHANGER?

INTERTECH(TM) HEAT AND MOISTURE EXCHANGER is a medical device that received FDA 510(k) clearance on 1990-12-13. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K903519.

When did INTERTECH(TM) HEAT AND MOISTURE EXCHANGER receive FDA 510(k) clearance?

INTERTECH(TM) HEAT AND MOISTURE EXCHANGER received FDA 510(k) clearance on 1990-12-13, under 510(k) number K903519.

Who is the listed applicant for INTERTECH(TM) HEAT AND MOISTURE EXCHANGER?

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

What is the FDA product code for INTERTECH(TM) HEAT AND MOISTURE EXCHANGER?

The FDA product code for INTERTECH(TM) HEAT AND MOISTURE EXCHANGER 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.

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 Intertech Resources, 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.

K9613181ST RESPONSE DISPOSABLE MANOMETERK955008HEAT & MOISTURE EXCHANGERK953580HEAT MOISTURE EXCHANGERK952223XENON GAS BREATHING CIRCUITK952062PFT FILTERK952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC

View all 29 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.

K955008HEAT & MOISTURE EXCHANGERIntertech Resources, Inc.K954194DISPOSABLE HME/FILTEREngstrom MedicalK953580HEAT MOISTURE EXCHANGERIntertech Resources, Inc.K953507TYPE 1 & 2 (HUMIDAIR I & II)Icor ABK953544HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHTGibeck, Inc.K953620WARM N WET HMEF W/LUER ADAPTERHospitak, 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.

↑