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FDA 510(k)

IV HOUSE

K-Number: K912942 · 1991-09-25

ApplicantProgressive Iv'S, Inc.
Decision Date1991-09-25
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV HOUSE is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Iv'S, Inc.. It received FDA 510(k) clearance on 1991-09-25 under 510(k) number K912942. 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 IV HOUSE?

IV HOUSE is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is Progressive Iv'S, Inc.. The 510(k) number is K912942.

When did IV HOUSE receive FDA 510(k) clearance?

IV HOUSE received FDA 510(k) clearance on 1991-09-25, under 510(k) number K912942.

Who is the listed applicant for IV HOUSE?

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

What is the FDA product code for IV HOUSE?

The FDA product code for IV HOUSE is KMK.

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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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