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FDA 510(k)

ZEISS VISULAS DIODE LASER

K-Number: K923274 · 1993-04-05

ApplicantCarl Zeiss, Inc.
Decision Date1993-04-05
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ZEISS VISULAS DIODE 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 1993-04-05 under 510(k) number K923274. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEISS VISULAS DIODE LASER?

ZEISS VISULAS DIODE LASER is a medical device that received FDA 510(k) clearance on 1993-04-05. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K923274.

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

ZEISS VISULAS DIODE LASER received FDA 510(k) clearance on 1993-04-05, under 510(k) number K923274.

Who is the listed applicant for ZEISS VISULAS DIODE 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 DIODE LASER?

The FDA product code for ZEISS VISULAS DIODE LASER is GEX. This falls under the Gastroenterology category.

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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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