FOCUS
K-Number: K002147 · 2000-10-13
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Device Summary
Frequently Asked Questions
What is the FOCUS?
FOCUS is a medical device that received FDA 510(k) clearance on 2000-10-13. The listed applicant is Computerized Medical Systems, Inc.. The 510(k) number is K002147.
When did FOCUS receive FDA 510(k) clearance?
FOCUS received FDA 510(k) clearance on 2000-10-13, under 510(k) number K002147.
Who is the listed applicant for FOCUS?
The FDA 510(k) record lists Computerized Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOCUS?
The FDA product code for FOCUS is MUJ.
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 PubMed Literature
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 Computerized Medical 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: MUJ)
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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