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FDA 510(k)

FREEVENT (TM)

K-Number: K903057 · 1990-11-20

ApplicantPharma Systems, Inc.
Decision Date1990-11-20
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FREEVENT (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Pharma Systems, Inc.. It received FDA 510(k) clearance on 1990-11-20 under 510(k) number K903057. 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 FREEVENT (TM)?

FREEVENT (TM) is a medical device that received FDA 510(k) clearance on 1990-11-20. The listed applicant is Pharma Systems, Inc.. The 510(k) number is K903057.

When did FREEVENT (TM) receive FDA 510(k) clearance?

FREEVENT (TM) received FDA 510(k) clearance on 1990-11-20, under 510(k) number K903057.

Who is the listed applicant for FREEVENT (TM)?

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

What is the FDA product code for FREEVENT (TM)?

The FDA product code for FREEVENT (TM) 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 Pharma Systems, 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.

K903055EXTENDED LIFE CIRCUITSK903058BACT-HME (TM)K903056BACTTRAPK903054HME-10 (TM)

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.

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