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FDA 510(k)

VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM

K-Number: K910005 · 1991-03-13

Decision Date1991-03-13
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM 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 1991-03-13 under 510(k) number K910005. 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(TM) M.R.I. VASCULAR ACCESS SYSTEM?

VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM is a medical device that received FDA 510(k) clearance on 1991-03-13. The listed applicant is Med Institute, Inc.. The 510(k) number is K910005.

When did VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM receive FDA 510(k) clearance?

VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM received FDA 510(k) clearance on 1991-03-13, under 510(k) number K910005.

Who is the listed applicant for VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM?

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(TM) M.R.I. VASCULAR ACCESS SYSTEM?

The FDA product code for VITAL-PORT(TM) M.R.I. VASCULAR ACCESS SYSTEM 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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