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FDA 510(k)

VISUCAM

K-Number: K021787 · 2002-06-21

ApplicantCarl Zeiss Ophthalmic Systems, Inc.
Decision Date2002-06-21
Product CodeNFF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISUCAM is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Ophthalmic Systems, Inc.. It received FDA 510(k) clearance on 2002-06-21 under 510(k) number K021787. The device is classified under product code NFF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISUCAM?

VISUCAM is a medical device that received FDA 510(k) clearance on 2002-06-21. The listed applicant is Carl Zeiss Ophthalmic Systems, Inc.. The 510(k) number is K021787.

When did VISUCAM receive FDA 510(k) clearance?

VISUCAM received FDA 510(k) clearance on 2002-06-21, under 510(k) number K021787.

Who is the listed applicant for VISUCAM?

The FDA 510(k) record lists Carl Zeiss Ophthalmic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISUCAM?

The FDA product code for VISUCAM is NFF.

Related Clinical Trials

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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Other records listing Carl Zeiss Ophthalmic Systems, Inc. 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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