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FDA 510(k)

VISUCAM PRO NM

K-Number: K052268 · 2005-11-02

ApplicantCarl Zeiss Meditec, AG
Decision Date2005-11-02
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISUCAM PRO NM is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2005-11-02 under 510(k) number K052268. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISUCAM PRO NM?

VISUCAM PRO NM is a medical device that received FDA 510(k) clearance on 2005-11-02. The listed applicant is Carl Zeiss Meditec, AG. The 510(k) number is K052268.

When did VISUCAM PRO NM receive FDA 510(k) clearance?

VISUCAM PRO NM received FDA 510(k) clearance on 2005-11-02, under 510(k) number K052268.

Who is the listed applicant for VISUCAM PRO NM?

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

What is the FDA product code for VISUCAM PRO NM?

The FDA product code for VISUCAM PRO NM is HKI.

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Other records listing Carl Zeiss Meditec, AG as applicant

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Related Devices (Code: HKI)

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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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