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FDA 510(k)

TRIPLE LUMEN INFUSIONCATHETERS-

K-Number: K834615 · 1984-02-14

Decision Date1984-02-14
Product CodeJCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRIPLE LUMEN INFUSIONCATHETERS- is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1984-02-14 under 510(k) number K834615. The device is classified under product code JCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIPLE LUMEN INFUSIONCATHETERS-?

TRIPLE LUMEN INFUSIONCATHETERS- is a medical device that received FDA 510(k) clearance on 1984-02-14. The listed applicant is Medical Components, Inc.. The 510(k) number is K834615.

When did TRIPLE LUMEN INFUSIONCATHETERS- receive FDA 510(k) clearance?

TRIPLE LUMEN INFUSIONCATHETERS- received FDA 510(k) clearance on 1984-02-14, under 510(k) number K834615.

Who is the listed applicant for TRIPLE LUMEN INFUSIONCATHETERS-?

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

What is the FDA product code for TRIPLE LUMEN INFUSIONCATHETERS-?

The FDA product code for TRIPLE LUMEN INFUSIONCATHETERS- is JCY.

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 Components, 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 61 devices →

Related Devices (Code: JCY)

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.

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