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FDA 510(k)

VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.

K-Number: K921201 · 1992-07-21

Decision Date1992-07-21
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST. is the device name listed in this FDA 510(k) record. The listed applicant is Med Institute, Inc.. It received FDA 510(k) clearance on 1992-07-21 under 510(k) number K921201. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.?

VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST. is a medical device that received FDA 510(k) clearance on 1992-07-21. The listed applicant is Med Institute, Inc.. The 510(k) number is K921201.

When did VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST. receive FDA 510(k) clearance?

VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST. received FDA 510(k) clearance on 1992-07-21, under 510(k) number K921201.

Who is the listed applicant for VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.?

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

What is the FDA product code for VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.?

The FDA product code for VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST. is LJT.

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 Med Institute, 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 26 devices →

Related Devices (Code: LJT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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