GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415
K-Number: K901832 · 1990-07-09
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Device Summary
Frequently Asked Questions
What is the GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415?
GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415 is a medical device that received FDA 510(k) clearance on 1990-07-09. The listed applicant is Amersham Corp.. The 510(k) number is K901832.
When did GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415 receive FDA 510(k) clearance?
GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415 received FDA 510(k) clearance on 1990-07-09, under 510(k) number K901832.
Who is the listed applicant for GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415?
The FDA 510(k) record lists Amersham Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415?
The FDA product code for GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415 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 Amersham 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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