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FDA 510(k)

K-LOK CATHETER SECUREMENT DEVICE

K-Number: K930225 · 1993-04-21

ApplicantK-Lok, Inc.
Decision Date1993-04-21
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

K-LOK CATHETER SECUREMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is K-Lok, Inc.. It received FDA 510(k) clearance on 1993-04-21 under 510(k) number K930225. 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 K-LOK CATHETER SECUREMENT DEVICE?

K-LOK CATHETER SECUREMENT DEVICE is a medical device that received FDA 510(k) clearance on 1993-04-21. The listed applicant is K-Lok, Inc.. The 510(k) number is K930225.

When did K-LOK CATHETER SECUREMENT DEVICE receive FDA 510(k) clearance?

K-LOK CATHETER SECUREMENT DEVICE received FDA 510(k) clearance on 1993-04-21, under 510(k) number K930225.

Who is the listed applicant for K-LOK CATHETER SECUREMENT DEVICE?

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

What is the FDA product code for K-LOK CATHETER SECUREMENT DEVICE?

The FDA product code for K-LOK CATHETER SECUREMENT DEVICE 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 K-Lok, 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.

K935252K-LOK CATHETER SECUREMENT DEVICE MODIFICATION

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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