SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM
K-Number: K896951 · 1990-02-26
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Device Summary
Frequently Asked Questions
What is the SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM?
SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Medisense, Inc.. The 510(k) number is K896951.
When did SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM receive FDA 510(k) clearance?
SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance on 1990-02-26, under 510(k) number K896951.
Who is the listed applicant for SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM?
The FDA 510(k) record lists Medisense, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM?
The FDA product code for SATELLITE G BLOOD GLUCOSE MONITORING SYSTEM is CGA.
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 Medisense, 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: CGA)
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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