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)

DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800

K-Number: K891753 · 1989-06-08

Decision Date1989-06-08
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800 is the device name listed in this FDA 510(k) record. The listed applicant is Akcess Medical Products, Inc.. It received FDA 510(k) clearance on 1989-06-08 under 510(k) number K891753. 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 DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800?

DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800 is a medical device that received FDA 510(k) clearance on 1989-06-08. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K891753.

When did DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800 receive FDA 510(k) clearance?

DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800 received FDA 510(k) clearance on 1989-06-08, under 510(k) number K891753.

Who is the listed applicant for DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800?

The FDA 510(k) record lists Akcess Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800?

The FDA product code for DUAL LUMEN SUB-CLAVIAN CATHETER, DLSC 600 & 800 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.

Other records listing Akcess Medical Products, 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 36 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.

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.

↑