VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.)
K-Number: K983544 · 1999-01-13
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Device Summary
Frequently Asked Questions
What is the VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.)?
VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.) is a medical device that received FDA 510(k) clearance on 1999-01-13. The listed applicant is Vygon Corp.. The 510(k) number is K983544.
When did VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.) receive FDA 510(k) clearance?
VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.) received FDA 510(k) clearance on 1999-01-13, under 510(k) number K983544.
Who is the listed applicant for VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.)?
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 VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.)?
The FDA product code for VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.) 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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