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FDA 510(k)

ZEISS VISULAS ARGON LASER

K-Number: K874609 · 1988-01-06

ApplicantCarl Zeiss, Inc.
Decision Date1988-01-06
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ZEISS VISULAS ARGON LASER 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 1988-01-06 under 510(k) number K874609. 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 ZEISS VISULAS ARGON LASER?

ZEISS VISULAS ARGON LASER is a medical device that received FDA 510(k) clearance on 1988-01-06. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K874609.

When did ZEISS VISULAS ARGON LASER receive FDA 510(k) clearance?

ZEISS VISULAS ARGON LASER received FDA 510(k) clearance on 1988-01-06, under 510(k) number K874609.

Who is the listed applicant for ZEISS VISULAS ARGON LASER?

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 ZEISS VISULAS ARGON LASER?

The FDA product code for ZEISS VISULAS ARGON LASER is HQF.

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Other records listing Carl Zeiss, Inc. as applicant

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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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