DENSITOMETER 18, COMPUTING, AUTO.
K-Number: K772325 · 1978-01-12
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Device Summary
Frequently Asked Questions
What is the DENSITOMETER 18, COMPUTING, AUTO.?
DENSITOMETER 18, COMPUTING, AUTO. is a medical device that received FDA 510(k) clearance on 1978-01-12. The listed applicant is Gelman Instrument Co.. The 510(k) number is K772325.
When did DENSITOMETER 18, COMPUTING, AUTO. receive FDA 510(k) clearance?
DENSITOMETER 18, COMPUTING, AUTO. received FDA 510(k) clearance on 1978-01-12, under 510(k) number K772325.
Who is the listed applicant for DENSITOMETER 18, COMPUTING, AUTO.?
The FDA 510(k) record lists Gelman Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENSITOMETER 18, COMPUTING, AUTO.?
The FDA product code for DENSITOMETER 18, COMPUTING, AUTO. is JQT.
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 Gelman Instrument Co. 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: JQT)
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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