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FDA 510(k)

PEGASUS WITH ACCESSORIES

K-Number: K903027 · 1990-10-02

ApplicantPfizer Laser Systems
Decision Date1990-10-02
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PEGASUS WITH ACCESSORIES 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 1990-10-02 under 510(k) number K903027. 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 PEGASUS WITH ACCESSORIES?

PEGASUS WITH ACCESSORIES is a medical device that received FDA 510(k) clearance on 1990-10-02. The listed applicant is Pfizer Laser Systems. The 510(k) number is K903027.

When did PEGASUS WITH ACCESSORIES receive FDA 510(k) clearance?

PEGASUS WITH ACCESSORIES received FDA 510(k) clearance on 1990-10-02, under 510(k) number K903027.

Who is the listed applicant for PEGASUS WITH ACCESSORIES?

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 PEGASUS WITH ACCESSORIES?

The FDA product code for PEGASUS WITH ACCESSORIES is GEX. This falls under the Gastroenterology category.

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Other records listing Pfizer Laser Systems as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: GEX)

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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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