SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010
K-Number: K023817 · 2003-06-25
Advertisement
Device Summary
Frequently Asked Questions
What is the SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010?
SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010 is a medical device that received FDA 510(k) clearance on 2003-06-25. The listed applicant is Clio Designs, Inc.. The 510(k) number is K023817.
When did SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010 receive FDA 510(k) clearance?
SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010 received FDA 510(k) clearance on 2003-06-25, under 510(k) number K023817.
Who is the listed applicant for SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010?
The FDA 510(k) record lists Clio Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010?
The FDA product code for SMARTSHAPE BODY COMPOSITION ANALYZER, MODEL 4010 is MNW.
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.
Related Devices (Code: MNW)
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.
Advertisement