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FDA 510(k)

I.V. FILTER HOLDER

K-Number: K832300 · 1983-10-04

ApplicantSaxnor Corp.
Decision Date1983-10-04
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. FILTER HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Saxnor Corp.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832300. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. FILTER HOLDER?

I.V. FILTER HOLDER is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Saxnor Corp.. The 510(k) number is K832300.

When did I.V. FILTER HOLDER receive FDA 510(k) clearance?

I.V. FILTER HOLDER received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832300.

Who is the listed applicant for I.V. FILTER HOLDER?

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

What is the FDA product code for I.V. FILTER HOLDER?

The FDA product code for I.V. FILTER HOLDER is KMK.

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 Saxnor Corp. 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.

K830300FREHAN INC. I.V. FILTER HOLDER

Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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