GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER
K-Number: K850260 · 1985-02-27
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Device Summary
Frequently Asked Questions
What is the GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER?
GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER is a medical device that received FDA 510(k) clearance on 1985-02-27. The listed applicant is Gelman Sciences, Inc.. The 510(k) number is K850260.
When did GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER receive FDA 510(k) clearance?
GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER received FDA 510(k) clearance on 1985-02-27, under 510(k) number K850260.
Who is the listed applicant for GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER?
The FDA 510(k) record lists Gelman Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER?
The FDA product code for GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER 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 Sciences, Inc. 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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