VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112
K-Number: K912423 · 1991-07-30
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Device Summary
Frequently Asked Questions
What is the VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112?
VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112 is a medical device that received FDA 510(k) clearance on 1991-07-30. The listed applicant is Med Institute, Inc.. The 510(k) number is K912423.
When did VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112 receive FDA 510(k) clearance?
VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112 received FDA 510(k) clearance on 1991-07-30, under 510(k) number K912423.
Who is the listed applicant for VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112?
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. VASCULAR ACCESS SYSTEM 7012,7112?
The FDA product code for VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112 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.
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
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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