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FDA 510(k)

CENTAURI/PEGASUS

K-Number: K905737 · 1991-06-17

ApplicantPfizer Laser Systems
Decision Date1991-06-17
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CENTAURI/PEGASUS is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer Laser Systems. It received FDA 510(k) clearance on 1991-06-17 under 510(k) number K905737. 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 CENTAURI/PEGASUS?

CENTAURI/PEGASUS is a medical device that received FDA 510(k) clearance on 1991-06-17. The listed applicant is Pfizer Laser Systems. The 510(k) number is K905737.

When did CENTAURI/PEGASUS receive FDA 510(k) clearance?

CENTAURI/PEGASUS received FDA 510(k) clearance on 1991-06-17, under 510(k) number K905737.

Who is the listed applicant for CENTAURI/PEGASUS?

The FDA 510(k) record lists Pfizer Laser Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTAURI/PEGASUS?

The FDA product code for CENTAURI/PEGASUS 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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