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FDA 510(k)

CARRIAZO PENDULAR

K-Number: K032910 · 2004-08-30

ApplicantSchwind Eye-Tech-Solutions GmbH & Co. KG
Decision Date2004-08-30
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CARRIAZO PENDULAR is the device name listed in this FDA 510(k) record. The listed applicant is Schwind Eye-Tech-Solutions GmbH & Co. KG. It received FDA 510(k) clearance on 2004-08-30 under 510(k) number K032910. 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 CARRIAZO PENDULAR?

CARRIAZO PENDULAR is a medical device that received FDA 510(k) clearance on 2004-08-30. The listed applicant is Schwind Eye-Tech-Solutions GmbH & Co. KG. The 510(k) number is K032910.

When did CARRIAZO PENDULAR receive FDA 510(k) clearance?

CARRIAZO PENDULAR received FDA 510(k) clearance on 2004-08-30, under 510(k) number K032910.

Who is the listed applicant for CARRIAZO PENDULAR?

The FDA 510(k) record lists Schwind Eye-Tech-Solutions GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARRIAZO PENDULAR?

The FDA product code for CARRIAZO PENDULAR is HNO.

Related Clinical Trials

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Other records listing Schwind Eye-Tech-Solutions GmbH & Co. KG 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.

K082043CARRIAZO-PENDULAR MICROKERATOME

Related Devices (Code: HNO)

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.

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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