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FDA 510(k)

STATLOCK SECUREMENT DEVICES

K-Number: K942931 · 1995-03-28

ApplicantVenetec, Inc.
Decision Date1995-03-28
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STATLOCK SECUREMENT DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Venetec, Inc.. It received FDA 510(k) clearance on 1995-03-28 under 510(k) number K942931. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STATLOCK SECUREMENT DEVICES?

STATLOCK SECUREMENT DEVICES is a medical device that received FDA 510(k) clearance on 1995-03-28. The listed applicant is Venetec, Inc.. The 510(k) number is K942931.

When did STATLOCK SECUREMENT DEVICES receive FDA 510(k) clearance?

STATLOCK SECUREMENT DEVICES received FDA 510(k) clearance on 1995-03-28, under 510(k) number K942931.

Who is the listed applicant for STATLOCK SECUREMENT DEVICES?

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 SECUREMENT DEVICES?

The FDA product code for STATLOCK SECUREMENT DEVICES is FPA.

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.

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.

Related Devices (Code: FPA)

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.

Official Source

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