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FDA 510(k)

MODIFIED VAS-CATH CATHETER REPAIR KIT

K-Number: K890099 · 1989-04-11

ApplicantVas-Cath, Inc.
Decision Date1989-04-11
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED VAS-CATH CATHETER REPAIR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Vas-Cath, Inc.. It received FDA 510(k) clearance on 1989-04-11 under 510(k) number K890099. 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 MODIFIED VAS-CATH CATHETER REPAIR KIT?

MODIFIED VAS-CATH CATHETER REPAIR KIT is a medical device that received FDA 510(k) clearance on 1989-04-11. The listed applicant is Vas-Cath, Inc.. The 510(k) number is K890099.

When did MODIFIED VAS-CATH CATHETER REPAIR KIT receive FDA 510(k) clearance?

MODIFIED VAS-CATH CATHETER REPAIR KIT received FDA 510(k) clearance on 1989-04-11, under 510(k) number K890099.

Who is the listed applicant for MODIFIED VAS-CATH CATHETER REPAIR KIT?

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

What is the FDA product code for MODIFIED VAS-CATH CATHETER REPAIR KIT?

The FDA product code for MODIFIED VAS-CATH CATHETER REPAIR KIT is LFJ.

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.

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Other records listing Vas-Cath, 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.

K973013OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETERK965178NIAGARA DUAL LUMEN CATHETERK964881ULTRAVERSE PTA CATHETERK970725OPTI-PLAST XL 5.5 F PTA CATHETERK941706OPTI-PLAST ANGIOPLASTY CATHETERK925485VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETER

View all 27 devices →

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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