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FDA 510(k)

CLEARCUT S SAFETY KNIFE

K-Number: K110166 · 2011-05-20

ApplicantAlcon Research, Ltd.
Decision Date2011-05-20
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CLEARCUT S SAFETY KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Research, Ltd.. It received FDA 510(k) clearance on 2011-05-20 under 510(k) number K110166. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARCUT S SAFETY KNIFE?

CLEARCUT S SAFETY KNIFE is a medical device that received FDA 510(k) clearance on 2011-05-20. The listed applicant is Alcon Research, Ltd.. The 510(k) number is K110166.

When did CLEARCUT S SAFETY KNIFE receive FDA 510(k) clearance?

CLEARCUT S SAFETY KNIFE received FDA 510(k) clearance on 2011-05-20, under 510(k) number K110166.

Who is the listed applicant for CLEARCUT S SAFETY KNIFE?

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

What is the FDA product code for CLEARCUT S SAFETY KNIFE?

The FDA product code for CLEARCUT S SAFETY KNIFE is HNN.

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Related Devices (Code: HNN)

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.

K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, Inc.K874056OPHTHALMIC DISPOSABLE BLADESMyocure, 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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