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FDA 510(k)

FPP IV SECURE

K-Number: K840683 · 1984-03-06

ApplicantFpp, Inc.
Decision Date1984-03-06
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FPP IV SECURE is the device name listed in this FDA 510(k) record. The listed applicant is Fpp, Inc.. It received FDA 510(k) clearance on 1984-03-06 under 510(k) number K840683. 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 FPP IV SECURE?

FPP IV SECURE is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is Fpp, Inc.. The 510(k) number is K840683.

When did FPP IV SECURE receive FDA 510(k) clearance?

FPP IV SECURE received FDA 510(k) clearance on 1984-03-06, under 510(k) number K840683.

Who is the listed applicant for FPP IV SECURE?

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

What is the FDA product code for FPP IV SECURE?

The FDA product code for FPP IV SECURE 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 Fpp, 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.

K840684FPP ARMBOARD STRAP

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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