PEGASUS
K-Number: K935009 · 1994-10-11
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Device Summary
Frequently Asked Questions
What is the PEGASUS?
PEGASUS is a medical device that received FDA 510(k) clearance on 1994-10-11. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K935009.
When did PEGASUS receive FDA 510(k) clearance?
PEGASUS received FDA 510(k) clearance on 1994-10-11, under 510(k) number K935009.
Who is the listed applicant for PEGASUS?
The FDA 510(k) record lists Advanced Technology Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PEGASUS?
The FDA product code for PEGASUS is IYN.
Related Clinical Trials
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.
Other records listing Advanced Technology Laboratories, Inc. 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.
Related Devices (Code: IYN)
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.
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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