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 UNIVERSAL HYDROPHOBIC FILTER

K-Number: K890346 · 1989-03-01

ApplicantIntertech/Ohio
Decision Date1989-03-01
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTERTECH UNIVERSAL HYDROPHOBIC FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Intertech/Ohio. It received FDA 510(k) clearance on 1989-03-01 under 510(k) number K890346. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERTECH UNIVERSAL HYDROPHOBIC FILTER?

INTERTECH UNIVERSAL HYDROPHOBIC FILTER is a medical device that received FDA 510(k) clearance on 1989-03-01. The listed applicant is Intertech/Ohio. The 510(k) number is K890346.

When did INTERTECH UNIVERSAL HYDROPHOBIC FILTER receive FDA 510(k) clearance?

INTERTECH UNIVERSAL HYDROPHOBIC FILTER received FDA 510(k) clearance on 1989-03-01, under 510(k) number K890346.

Who is the listed applicant for INTERTECH UNIVERSAL HYDROPHOBIC FILTER?

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

What is the FDA product code for INTERTECH UNIVERSAL HYDROPHOBIC FILTER?

The FDA product code for INTERTECH UNIVERSAL HYDROPHOBIC FILTER is CAH.

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/Ohio 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.

K895144INTERTECH METERED DOSE ELBOWK884525PEDIATRIC HUMIDIFIER TUBE W/ TEMPERATURE PORTK884526ADULT RESUSCITATOR WITH MASK AND FILTERK882204RESUSCITATOR VALVE ASSEMBLY W/FILTERK880394FIRST RESPONSE PEDIATRIC EMERGENCY RESUSCITATORK863033PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS

View all 10 devices →

Related Devices (Code: CAH)

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.

K252643Iso-Gard Filter Straight; Humid-Vent Filter Compact AngledTeleflex Medical Sdn. Bhd.K251583Ambu® Virobac II® Exhalation FilterAmbu A/SK241339Besmed Bacterial Filter and HMEFBesmed Health Business CorpK222917Breathing circuit bacterial/viral filterShaoxing Haitech Medical Products Co., Ltd.K230483Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15)Passy-Muir, Inc.K223258TNI Clear-Guard™ 3 angled breathing filter (1545020)Intersurgical , Ltd.

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.

↑