SPHYGMOCOR MX MODEL SCOR-MX
K-Number: K002742 · 2001-05-01
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Device Summary
Frequently Asked Questions
What is the SPHYGMOCOR MX MODEL SCOR-MX?
SPHYGMOCOR MX MODEL SCOR-MX is a medical device that received FDA 510(k) clearance on 2001-05-01. The listed applicant is Pwv Medical Pty, Lt.. The 510(k) number is K002742.
When did SPHYGMOCOR MX MODEL SCOR-MX receive FDA 510(k) clearance?
SPHYGMOCOR MX MODEL SCOR-MX received FDA 510(k) clearance on 2001-05-01, under 510(k) number K002742.
Who is the listed applicant for SPHYGMOCOR MX MODEL SCOR-MX?
The FDA 510(k) record lists Pwv Medical Pty, Lt. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPHYGMOCOR MX MODEL SCOR-MX?
The FDA product code for SPHYGMOCOR MX MODEL SCOR-MX is DSK.
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: DSK)
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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