DPX SERIES BRAVO DUO BONE DENSITOMETER
K-Number: K030962 · 2003-07-25
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Device Summary
Frequently Asked Questions
What is the DPX SERIES BRAVO DUO BONE DENSITOMETER?
DPX SERIES BRAVO DUO BONE DENSITOMETER is a medical device that received FDA 510(k) clearance on 2003-07-25. The listed applicant is Ge Lunar Corp.. The 510(k) number is K030962.
When did DPX SERIES BRAVO DUO BONE DENSITOMETER receive FDA 510(k) clearance?
DPX SERIES BRAVO DUO BONE DENSITOMETER received FDA 510(k) clearance on 2003-07-25, under 510(k) number K030962.
Who is the listed applicant for DPX SERIES BRAVO DUO BONE DENSITOMETER?
The FDA 510(k) record lists Ge Lunar Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DPX SERIES BRAVO DUO BONE DENSITOMETER?
The FDA product code for DPX SERIES BRAVO DUO BONE DENSITOMETER 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 Ge 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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