PRECISION Q I D BLOOD GLUCOSE TEST STRIPS
K-Number: K945887 · 1995-03-23
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Device Summary
Frequently Asked Questions
What is the PRECISION Q I D BLOOD GLUCOSE TEST STRIPS?
PRECISION Q I D BLOOD GLUCOSE TEST STRIPS is a medical device that received FDA 510(k) clearance on 1995-03-23. The listed applicant is Medisense, Inc.. The 510(k) number is K945887.
When did PRECISION Q I D BLOOD GLUCOSE TEST STRIPS receive FDA 510(k) clearance?
PRECISION Q I D BLOOD GLUCOSE TEST STRIPS received FDA 510(k) clearance on 1995-03-23, under 510(k) number K945887.
Who is the listed applicant for PRECISION Q I D BLOOD GLUCOSE TEST STRIPS?
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 PRECISION Q I D BLOOD GLUCOSE TEST STRIPS?
The FDA product code for PRECISION Q I D BLOOD GLUCOSE TEST STRIPS 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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