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FDA 510(k)

DISPOSABLE N-PE MICROKERATOME BLADES

K-Number: K022205 · 2002-10-03

ApplicantOasis Medical, Inc.
Decision Date2002-10-03
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE N-PE MICROKERATOME BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Oasis Medical, Inc.. It received FDA 510(k) clearance on 2002-10-03 under 510(k) number K022205. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE N-PE MICROKERATOME BLADES?

DISPOSABLE N-PE MICROKERATOME BLADES is a medical device that received FDA 510(k) clearance on 2002-10-03. The listed applicant is Oasis Medical, Inc.. The 510(k) number is K022205.

When did DISPOSABLE N-PE MICROKERATOME BLADES receive FDA 510(k) clearance?

DISPOSABLE N-PE MICROKERATOME BLADES received FDA 510(k) clearance on 2002-10-03, under 510(k) number K022205.

Who is the listed applicant for DISPOSABLE N-PE MICROKERATOME BLADES?

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

What is the FDA product code for DISPOSABLE N-PE MICROKERATOME BLADES?

The FDA product code for DISPOSABLE N-PE MICROKERATOME BLADES is HNO.

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Other records listing Oasis Medical, Inc. as applicant

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Related Devices (Code: HNO)

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K173371VisuMax Femtosecond LaserCarl Zeiss Meditec, Inc.K172994EPI K ConsoleMoria SAK072102EPIVISION SL SYSTEMGebauer Medizintechnik GmbHK082043CARRIAZO-PENDULAR MICROKERATOMESchwind Eye-Tech-Solutions GmbH & Co. KGK062465ZYOPTIX XP EPI SEPARATOR SYSTEMBausch & Lomb, Inc.K052891HORIZON EPIKERATOME DISPOSABLE MICROKERATOME SYSTEMHawken Industries

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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