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)

UNIVERSAL IRRIGATION & SUCTION TUBING SET

K-Number: K922714 · 1993-08-03

Decision Date1993-08-03
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL IRRIGATION & SUCTION TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Ximed Medical Systems. It received FDA 510(k) clearance on 1993-08-03 under 510(k) number K922714. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL IRRIGATION & SUCTION TUBING SET?

UNIVERSAL IRRIGATION & SUCTION TUBING SET is a medical device that received FDA 510(k) clearance on 1993-08-03. The listed applicant is Ximed Medical Systems. The 510(k) number is K922714.

When did UNIVERSAL IRRIGATION & SUCTION TUBING SET receive FDA 510(k) clearance?

UNIVERSAL IRRIGATION & SUCTION TUBING SET received FDA 510(k) clearance on 1993-08-03, under 510(k) number K922714.

Who is the listed applicant for UNIVERSAL IRRIGATION & SUCTION TUBING SET?

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

What is the FDA product code for UNIVERSAL IRRIGATION & SUCTION TUBING SET?

The FDA product code for UNIVERSAL IRRIGATION & SUCTION TUBING SET is JOL.

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 Ximed Medical Systems 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 11 devices →

Related Devices (Code: JOL)

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.

↑