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FDA 510(k)

DOUBLE LUMEN SUBCLAVIN CATHETER SC-400

K-Number: K810745 · 1981-03-31

ApplicantVas-Cath of Canada , Ltd.
Decision Date1981-03-31
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DOUBLE LUMEN SUBCLAVIN CATHETER SC-400 is the device name listed in this FDA 510(k) record. The listed applicant is Vas-Cath of Canada , Ltd.. It received FDA 510(k) clearance on 1981-03-31 under 510(k) number K810745. 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 DOUBLE LUMEN SUBCLAVIN CATHETER SC-400?

DOUBLE LUMEN SUBCLAVIN CATHETER SC-400 is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K810745.

When did DOUBLE LUMEN SUBCLAVIN CATHETER SC-400 receive FDA 510(k) clearance?

DOUBLE LUMEN SUBCLAVIN CATHETER SC-400 received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810745.

Who is the listed applicant for DOUBLE LUMEN SUBCLAVIN CATHETER SC-400?

The FDA 510(k) record lists Vas-Cath of Canada , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOUBLE LUMEN SUBCLAVIN CATHETER SC-400?

The FDA product code for DOUBLE LUMEN SUBCLAVIN CATHETER SC-400 is LFJ.

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Other records listing Vas-Cath of Canada , Ltd. 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.

K875188LUER LOCK CONNECTORS / RIDIG P.V.C.K871817VAS-CATH PERITONEAL DIALYSIS CATHETERK871487VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATHK871488VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATHK863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYK853283VACCESS TM 4006

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Related Devices (Code: LFJ)

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.

K920780MEDSURG INSERTION TRAYMedsurg Industries, Inc.K925819AKCESS0CATH KITAkcess Medical Products, Inc.K925818AKCESS-CATHAkcess Medical Products, Inc.K913468ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET/TRAYCook, Inc.K931120COAXIAL ACUTE CATHETERAkcess Medical Products, Inc.K920634SPLITTABLE SHEATH INTRODUCER SETAkcess Medical Products, Inc.

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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