LC SPRINT STAR
K-Number: K062158 · 2006-08-28
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Device Summary
Frequently Asked Questions
What is the LC SPRINT STAR?
LC SPRINT STAR is a medical device that received FDA 510(k) clearance on 2006-08-28. The listed applicant is Pari Innovative Manufacturers, Inc.. The 510(k) number is K062158.
When did LC SPRINT STAR receive FDA 510(k) clearance?
LC SPRINT STAR received FDA 510(k) clearance on 2006-08-28, under 510(k) number K062158.
Who is the listed applicant for LC SPRINT STAR?
The FDA 510(k) record lists Pari Innovative Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LC SPRINT STAR?
The FDA product code for LC SPRINT STAR is CAF.
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 Pari Innovative Manufacturers, 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: CAF)
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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