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FDA 510(k)

GENNY DENNY IV SHIELD

K-Number: K905735 · 1991-01-18

ApplicantTadco, Inc.
Decision Date1991-01-18
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GENNY DENNY IV SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Tadco, Inc.. It received FDA 510(k) clearance on 1991-01-18 under 510(k) number K905735. 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 GENNY DENNY IV SHIELD?

GENNY DENNY IV SHIELD is a medical device that received FDA 510(k) clearance on 1991-01-18. The listed applicant is Tadco, Inc.. The 510(k) number is K905735.

When did GENNY DENNY IV SHIELD receive FDA 510(k) clearance?

GENNY DENNY IV SHIELD received FDA 510(k) clearance on 1991-01-18, under 510(k) number K905735.

Who is the listed applicant for GENNY DENNY IV SHIELD?

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

What is the FDA product code for GENNY DENNY IV SHIELD?

The FDA product code for GENNY DENNY IV SHIELD 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.

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Other records listing Tadco, 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.

K926158SLATER SLEEVE

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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