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FDA 510(k)

MODIFICATION HEMOFILTRATION CATHETER HF-100

K-Number: K890717 · 1989-04-05

ApplicantVas-Cath, Inc.
Decision Date1989-04-05
Product CodeLFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION HEMOFILTRATION CATHETER HF-100 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 1989-04-05 under 510(k) number K890717. The device is classified under product code LFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION HEMOFILTRATION CATHETER HF-100?

MODIFICATION HEMOFILTRATION CATHETER HF-100 is a medical device that received FDA 510(k) clearance on 1989-04-05. The listed applicant is Vas-Cath, Inc.. The 510(k) number is K890717.

When did MODIFICATION HEMOFILTRATION CATHETER HF-100 receive FDA 510(k) clearance?

MODIFICATION HEMOFILTRATION CATHETER HF-100 received FDA 510(k) clearance on 1989-04-05, under 510(k) number K890717.

Who is the listed applicant for MODIFICATION HEMOFILTRATION CATHETER HF-100?

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 MODIFICATION HEMOFILTRATION CATHETER HF-100?

The FDA product code for MODIFICATION HEMOFILTRATION CATHETER HF-100 is LFK.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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: LFK)

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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)Medron, Inc.K914936CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SETAkcess Medical Products, Inc.K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSAkcess Medical Products, Inc.K891764FC-101 FEMORAL CATHETER GUIDE WIREAkcess Medical Products, Inc.K891763FC-100 FEMORAL CATHETERAkcess Medical Products, Inc.K880775CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAYMedsurg Industries, 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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