IQ BODY FLUIDS CONTROL
K-Number: K051706 · 2005-08-17
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Device Summary
Frequently Asked Questions
What is the IQ BODY FLUIDS CONTROL?
IQ BODY FLUIDS CONTROL is a medical device that received FDA 510(k) clearance on 2005-08-17. The listed applicant is Streck. The 510(k) number is K051706.
When did IQ BODY FLUIDS CONTROL receive FDA 510(k) clearance?
IQ BODY FLUIDS CONTROL received FDA 510(k) clearance on 2005-08-17, under 510(k) number K051706.
Who is the listed applicant for IQ BODY FLUIDS CONTROL?
The FDA 510(k) record lists Streck as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IQ BODY FLUIDS CONTROL?
The FDA product code for IQ BODY FLUIDS CONTROL is JPK.
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 Streck 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: JPK)
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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