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)

PERCUTANEOUS NEPHROSTOMY CATHETER

K-Number: K833008 · 1983-10-19

Decision Date1983-10-19
Product CodeLJE
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS NEPHROSTOMY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering Corp.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K833008. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUTANEOUS NEPHROSTOMY CATHETER?

PERCUTANEOUS NEPHROSTOMY CATHETER is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Medical Engineering Corp.. The 510(k) number is K833008.

When did PERCUTANEOUS NEPHROSTOMY CATHETER receive FDA 510(k) clearance?

PERCUTANEOUS NEPHROSTOMY CATHETER received FDA 510(k) clearance on 1983-10-19, under 510(k) number K833008.

Who is the listed applicant for PERCUTANEOUS NEPHROSTOMY CATHETER?

The FDA 510(k) record lists Medical Engineering Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERCUTANEOUS NEPHROSTOMY CATHETER?

The FDA product code for PERCUTANEOUS NEPHROSTOMY CATHETER is LJE.

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 Medical Engineering Corp. 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 28 devices →

Related Devices (Code: LJE)

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.

↑