VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P
K-Number: K924748 · 1993-07-28
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Device Summary
Frequently Asked Questions
What is the VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P?
VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P is a medical device that received FDA 510(k) clearance on 1993-07-28. The listed applicant is Med Institute, Inc.. The 510(k) number is K924748.
When did VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P receive FDA 510(k) clearance?
VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P received FDA 510(k) clearance on 1993-07-28, under 510(k) number K924748.
Who is the listed applicant for VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P?
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 VASC ACCESS 901OP/911OP/9012P/9112P?
The FDA product code for VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P 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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