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FDA 510(k)

CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)

K-Number: K000637 · 2000-05-19

ApplicantAlcon Laboratories, Inc.
Decision Date2000-05-19
Product CodeNCF
Advisory CommitteeOP
DecisionUnknown

Device Summary

CUSTOMCORNEA MEASUREMENT DEVICE (CCMD) is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2000-05-19 under 510(k) number K000637. The device is classified under product code NCF. It was reviewed by the OP advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)?

CUSTOMCORNEA MEASUREMENT DEVICE (CCMD) is a medical device that received FDA 510(k) clearance on 2000-05-19. The listed applicant is Alcon Laboratories, Inc.. The 510(k) number is K000637.

When did CUSTOMCORNEA MEASUREMENT DEVICE (CCMD) receive FDA 510(k) clearance?

CUSTOMCORNEA MEASUREMENT DEVICE (CCMD) received FDA 510(k) clearance on 2000-05-19, under 510(k) number K000637.

Who is the listed applicant for CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)?

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

What is the FDA product code for CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)?

The FDA product code for CUSTOMCORNEA MEASUREMENT DEVICE (CCMD) is NCF.

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Other records listing Alcon Laboratories, Inc. as applicant

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Related Devices (Code: NCF)

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.

K062930LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEMAlcon Research, Ltd.K050336OPD-STATION SOFTWARENidek, Inc.K023249ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEMAlcon Laboratories, 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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