Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VASCULAR ACCESS CATH. REPAIR KIT

K-Number: K833915 · 1984-03-30

Decision Date1984-03-30
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VASCULAR ACCESS CATH. REPAIR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K833915. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR ACCESS CATH. REPAIR KIT?

VASCULAR ACCESS CATH. REPAIR KIT is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. The 510(k) number is K833915.

When did VASCULAR ACCESS CATH. REPAIR KIT receive FDA 510(k) clearance?

VASCULAR ACCESS CATH. REPAIR KIT received FDA 510(k) clearance on 1984-03-30, under 510(k) number K833915.

Who is the listed applicant for VASCULAR ACCESS CATH. REPAIR KIT?

The FDA 510(k) record lists Cormed, Inc., Sub. C.R.Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCULAR ACCESS CATH. REPAIR KIT?

The FDA product code for VASCULAR ACCESS CATH. REPAIR KIT 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 Cormed, Inc., Sub. C.R.Bard, 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.

View all 8 devices →

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.

↑