LIFECATH S PICC AND MIDLINE CATHETER
K-Number: K062425 · 2006-09-15
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Device Summary
Frequently Asked Questions
What is the LIFECATH S PICC AND MIDLINE CATHETER?
LIFECATH S PICC AND MIDLINE CATHETER is a medical device that received FDA 510(k) clearance on 2006-09-15. The listed applicant is Vygon Corp.. The 510(k) number is K062425.
When did LIFECATH S PICC AND MIDLINE CATHETER receive FDA 510(k) clearance?
LIFECATH S PICC AND MIDLINE CATHETER received FDA 510(k) clearance on 2006-09-15, under 510(k) number K062425.
Who is the listed applicant for LIFECATH S PICC AND MIDLINE CATHETER?
The FDA 510(k) record lists Vygon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIFECATH S PICC AND MIDLINE CATHETER?
The FDA product code for LIFECATH S PICC AND MIDLINE CATHETER is LJS.
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 Vygon Corp. 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: LJS)
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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