FLOUROMETER/DENSITOMETER MODEL 720
K-Number: K770026 · 1977-01-26
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Device Summary
Frequently Asked Questions
What is the FLOUROMETER/DENSITOMETER MODEL 720?
FLOUROMETER/DENSITOMETER MODEL 720 is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Corning Medical & Scientific. The 510(k) number is K770026.
When did FLOUROMETER/DENSITOMETER MODEL 720 receive FDA 510(k) clearance?
FLOUROMETER/DENSITOMETER MODEL 720 received FDA 510(k) clearance on 1977-01-26, under 510(k) number K770026.
Who is the listed applicant for FLOUROMETER/DENSITOMETER MODEL 720?
The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOUROMETER/DENSITOMETER MODEL 720?
The FDA product code for FLOUROMETER/DENSITOMETER MODEL 720 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 Corning Medical & Scientific 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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