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FDA 510(k)

DORNIER MEDILAS FIBER TOME LASER

K-Number: K964760 · 1997-02-19

ApplicantDornier Medtech America, Inc.
Decision Date1997-02-19
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DORNIER MEDILAS FIBER TOME LASER is the device name listed in this FDA 510(k) record. The listed applicant is Dornier Medtech America, Inc.. It received FDA 510(k) clearance on 1997-02-19 under 510(k) number K964760. 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 DORNIER MEDILAS FIBER TOME LASER?

DORNIER MEDILAS FIBER TOME LASER is a medical device that received FDA 510(k) clearance on 1997-02-19. The listed applicant is Dornier Medtech America, Inc.. The 510(k) number is K964760.

When did DORNIER MEDILAS FIBER TOME LASER receive FDA 510(k) clearance?

DORNIER MEDILAS FIBER TOME LASER received FDA 510(k) clearance on 1997-02-19, under 510(k) number K964760.

Who is the listed applicant for DORNIER MEDILAS FIBER TOME LASER?

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

What is the FDA product code for DORNIER MEDILAS FIBER TOME LASER?

The FDA product code for DORNIER MEDILAS FIBER TOME LASER is GEX. This falls under the Gastroenterology category.

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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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