LEGACY/LEGACY-D TABLE
K-Number: K973039 · 1997-10-16
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Device Summary
Frequently Asked Questions
What is the LEGACY/LEGACY-D TABLE?
LEGACY/LEGACY-D TABLE is a medical device that received FDA 510(k) clearance on 1997-10-16. The listed applicant is GE Medical Systems. The 510(k) number is K973039.
When did LEGACY/LEGACY-D TABLE receive FDA 510(k) clearance?
LEGACY/LEGACY-D TABLE received FDA 510(k) clearance on 1997-10-16, under 510(k) number K973039.
Who is the listed applicant for LEGACY/LEGACY-D TABLE?
The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEGACY/LEGACY-D TABLE?
The FDA product code for LEGACY/LEGACY-D TABLE is IXR.
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 GE Medical 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.
Related Devices (Code: IXR)
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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