MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY
K-Number: K974308 · 1998-01-27
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Device Summary
Frequently Asked Questions
What is the MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY?
MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY is a medical device that received FDA 510(k) clearance on 1998-01-27. The listed applicant is Medrad, Inc.. The 510(k) number is K974308.
When did MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY receive FDA 510(k) clearance?
MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY received FDA 510(k) clearance on 1998-01-27, under 510(k) number K974308.
Who is the listed applicant for MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY?
The FDA 510(k) record lists Medrad, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY?
The FDA product code for MEDRAD 1.5T PERIPHERAL VASCULAR ARRAY is MOS.
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 Medrad, 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: MOS)
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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