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FDA 510(k)

I.V. STRIP

K-Number: K792049 · 1979-11-20

ApplicantE-Med Corp.
Decision Date1979-11-20
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. STRIP is the device name listed in this FDA 510(k) record. The listed applicant is E-Med Corp.. It received FDA 510(k) clearance on 1979-11-20 under 510(k) number K792049. 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. STRIP?

I.V. STRIP is a medical device that received FDA 510(k) clearance on 1979-11-20. The listed applicant is E-Med Corp.. The 510(k) number is K792049.

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

I.V. STRIP received FDA 510(k) clearance on 1979-11-20, under 510(k) number K792049.

Who is the listed applicant for I.V. STRIP?

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

What is the FDA product code for I.V. STRIP?

The FDA product code for I.V. STRIP 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 E-Med 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.

K971619MICROFUSE MEMBRANE INFUSION CATHETERK843200SITE STRIP

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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