PEDIATRIC REFERENCE DATA
K-Number: K001812 · 2000-07-10
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Device Summary
Frequently Asked Questions
What is the PEDIATRIC REFERENCE DATA?
PEDIATRIC REFERENCE DATA is a medical device that received FDA 510(k) clearance on 2000-07-10. The listed applicant is Lunar Corp.. The 510(k) number is K001812.
When did PEDIATRIC REFERENCE DATA receive FDA 510(k) clearance?
PEDIATRIC REFERENCE DATA received FDA 510(k) clearance on 2000-07-10, under 510(k) number K001812.
Who is the listed applicant for PEDIATRIC REFERENCE DATA?
The FDA 510(k) record lists Lunar Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PEDIATRIC REFERENCE DATA?
The FDA product code for PEDIATRIC REFERENCE DATA is KGI.
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 Lunar Corp. 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: KGI)
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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