GLUCOSE-HK REAGENT
K-Number: K873835 · 1987-11-24
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Device Summary
Frequently Asked Questions
What is the GLUCOSE-HK REAGENT?
GLUCOSE-HK REAGENT is a medical device that received FDA 510(k) clearance on 1987-11-24. The listed applicant is Intersect Systems, Inc.. The 510(k) number is K873835.
When did GLUCOSE-HK REAGENT receive FDA 510(k) clearance?
GLUCOSE-HK REAGENT received FDA 510(k) clearance on 1987-11-24, under 510(k) number K873835.
Who is the listed applicant for GLUCOSE-HK REAGENT?
The FDA 510(k) record lists Intersect Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLUCOSE-HK REAGENT?
The FDA product code for GLUCOSE-HK REAGENT is CFR.
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 Intersect Systems, 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: CFR)
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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