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FDA 510(k)

STATLOCK CV

K-Number: K943147 · 1994-09-29

ApplicantVenetec, Inc.
Decision Date1994-09-29
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STATLOCK CV is the device name listed in this FDA 510(k) record. The listed applicant is Venetec, Inc.. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K943147. 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 STATLOCK CV?

STATLOCK CV is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Venetec, Inc.. The 510(k) number is K943147.

When did STATLOCK CV receive FDA 510(k) clearance?

STATLOCK CV received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943147.

Who is the listed applicant for STATLOCK CV?

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

What is the FDA product code for STATLOCK CV?

The FDA product code for STATLOCK CV 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 Venetec, 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.

K943038STATLOCK-IPIDURALK942931STATLOCK SECUREMENT DEVICESK902109STATLOCK IV CONNECTOR AND ANCHOR SET

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.K943047IV START KITSSterile Concepts, Inc.K941850IMMOBILE NON-STERILE AND IMMOBILE A/C NON-STERILETnt Moborg Intl. , Ltd.

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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