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FDA 510(k)

DUALYSE-CATH - CODES #1132.212, 1132.112

K-Number: K896568 · 1990-05-09

ApplicantVygon Corp.
Decision Date1990-05-09
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DUALYSE-CATH - CODES #1132.212, 1132.112 is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1990-05-09 under 510(k) number K896568. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUALYSE-CATH - CODES #1132.212, 1132.112?

DUALYSE-CATH - CODES #1132.212, 1132.112 is a medical device that received FDA 510(k) clearance on 1990-05-09. The listed applicant is Vygon Corp.. The 510(k) number is K896568.

When did DUALYSE-CATH - CODES #1132.212, 1132.112 receive FDA 510(k) clearance?

DUALYSE-CATH - CODES #1132.212, 1132.112 received FDA 510(k) clearance on 1990-05-09, under 510(k) number K896568.

Who is the listed applicant for DUALYSE-CATH - CODES #1132.212, 1132.112?

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 DUALYSE-CATH - CODES #1132.212, 1132.112?

The FDA product code for DUALYSE-CATH - CODES #1132.212, 1132.112 is LFJ.

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Related Devices (Code: LFJ)

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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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