DPX BONE DENSITOMETER
K-Number: K873296 · 1988-06-06
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Device Summary
Frequently Asked Questions
What is the DPX BONE DENSITOMETER?
DPX BONE DENSITOMETER is a medical device that received FDA 510(k) clearance on 1988-06-06. The listed applicant is Lunar Radiation Corp.. The 510(k) number is K873296.
When did DPX BONE DENSITOMETER receive FDA 510(k) clearance?
DPX BONE DENSITOMETER received FDA 510(k) clearance on 1988-06-06, under 510(k) number K873296.
Who is the listed applicant for DPX BONE DENSITOMETER?
The FDA 510(k) record lists Lunar Radiation Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DPX BONE DENSITOMETER?
The FDA product code for DPX 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 Lunar Radiation 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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