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FDA 510(k)

QUAD-LINK RETRACTABLE MOUNT

K-Number: K911152 · 1991-03-26

Decision Date1991-03-26
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUAD-LINK RETRACTABLE MOUNT is the device name listed in this FDA 510(k) record. The listed applicant is Tarsys Engineering, Inc.. It received FDA 510(k) clearance on 1991-03-26 under 510(k) number K911152. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUAD-LINK RETRACTABLE MOUNT?

QUAD-LINK RETRACTABLE MOUNT is a medical device that received FDA 510(k) clearance on 1991-03-26. The listed applicant is Tarsys Engineering, Inc.. The 510(k) number is K911152.

When did QUAD-LINK RETRACTABLE MOUNT receive FDA 510(k) clearance?

QUAD-LINK RETRACTABLE MOUNT received FDA 510(k) clearance on 1991-03-26, under 510(k) number K911152.

Who is the listed applicant for QUAD-LINK RETRACTABLE MOUNT?

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

What is the FDA product code for QUAD-LINK RETRACTABLE MOUNT?

The FDA product code for QUAD-LINK RETRACTABLE MOUNT is ITI.

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 Tarsys Engineering, 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: ITI)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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