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FDA 510(k)

VISULINK 900 ARGON

K-Number: K952894 · 1995-08-14

ApplicantCarl Zeiss, Inc.
Decision Date1995-08-14
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISULINK 900 ARGON is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss, Inc.. It received FDA 510(k) clearance on 1995-08-14 under 510(k) number K952894. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISULINK 900 ARGON?

VISULINK 900 ARGON is a medical device that received FDA 510(k) clearance on 1995-08-14. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K952894.

When did VISULINK 900 ARGON receive FDA 510(k) clearance?

VISULINK 900 ARGON received FDA 510(k) clearance on 1995-08-14, under 510(k) number K952894.

Who is the listed applicant for VISULINK 900 ARGON?

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

What is the FDA product code for VISULINK 900 ARGON?

The FDA product code for VISULINK 900 ARGON is HQF.

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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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