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FDA 510(k)

STENTUBE LACRIMAL INTUBATION SET

K-Number: K113118 · 2012-07-31

ApplicantQuest Medical, Inc.
Decision Date2012-07-31
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

STENTUBE LACRIMAL INTUBATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Quest Medical, Inc.. It received FDA 510(k) clearance on 2012-07-31 under 510(k) number K113118. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STENTUBE LACRIMAL INTUBATION SET?

STENTUBE LACRIMAL INTUBATION SET is a medical device that received FDA 510(k) clearance on 2012-07-31. The listed applicant is Quest Medical, Inc.. The 510(k) number is K113118.

When did STENTUBE LACRIMAL INTUBATION SET receive FDA 510(k) clearance?

STENTUBE LACRIMAL INTUBATION SET received FDA 510(k) clearance on 2012-07-31, under 510(k) number K113118.

Who is the listed applicant for STENTUBE LACRIMAL INTUBATION SET?

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

What is the FDA product code for STENTUBE LACRIMAL INTUBATION SET?

The FDA product code for STENTUBE LACRIMAL INTUBATION SET is OKS.

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Related Devices (Code: OKS)

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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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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