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)

CLOSED DISCONNECT SYSTEM

K-Number: K900106 · 1990-07-16

ApplicantDelmed, Inc.
Decision Date1990-07-16
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLOSED DISCONNECT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Delmed, Inc.. It received FDA 510(k) clearance on 1990-07-16 under 510(k) number K900106. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLOSED DISCONNECT SYSTEM?

CLOSED DISCONNECT SYSTEM is a medical device that received FDA 510(k) clearance on 1990-07-16. The listed applicant is Delmed, Inc.. The 510(k) number is K900106.

When did CLOSED DISCONNECT SYSTEM receive FDA 510(k) clearance?

CLOSED DISCONNECT SYSTEM received FDA 510(k) clearance on 1990-07-16, under 510(k) number K900106.

Who is the listed applicant for CLOSED DISCONNECT SYSTEM?

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

What is the FDA product code for CLOSED DISCONNECT SYSTEM?

The FDA product code for CLOSED DISCONNECT SYSTEM is KDJ.

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 Delmed, 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 27 devices →

Related Devices (Code: KDJ)

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.

↑