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FDA 510(k)

EAGLESOFT CHAIRSIDE

K-Number: K982422 · 1998-09-30

ApplicantEaglesoft, A Patterson Co.
Decision Date1998-09-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EAGLESOFT CHAIRSIDE is the device name listed in this FDA 510(k) record. The listed applicant is Eaglesoft, A Patterson Co.. It received FDA 510(k) clearance on 1998-09-30 under 510(k) number K982422. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLESOFT CHAIRSIDE?

EAGLESOFT CHAIRSIDE is a medical device that received FDA 510(k) clearance on 1998-09-30. The listed applicant is Eaglesoft, A Patterson Co.. The 510(k) number is K982422.

When did EAGLESOFT CHAIRSIDE receive FDA 510(k) clearance?

EAGLESOFT CHAIRSIDE received FDA 510(k) clearance on 1998-09-30, under 510(k) number K982422.

Who is the listed applicant for EAGLESOFT CHAIRSIDE?

The FDA 510(k) record lists Eaglesoft, A Patterson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EAGLESOFT CHAIRSIDE?

The FDA product code for EAGLESOFT CHAIRSIDE is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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