EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE SYSTEM
K-Number: K043245 · 2005-04-29
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Device Summary
Frequently Asked Questions
What is the EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE SYSTEM?
EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE SYSTEM is a medical device that received FDA 510(k) clearance on 2005-04-29. The listed applicant is Eps Bio Technology Corp.. The 510(k) number is K043245.
When did EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE SYSTEM receive FDA 510(k) clearance?
EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE SYSTEM received FDA 510(k) clearance on 2005-04-29, under 510(k) number K043245.
Who is the listed applicant for EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE SYSTEM?
The FDA 510(k) record lists Eps Bio Technology Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE SYSTEM?
The FDA product code for EPS EASY PAIN SUPREME SELF MONITORING BLOOD GLUCOSE 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 Eps Bio Technology Corp. 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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