DYNAMIC CARDIAC PHANTOM 74-347
K-Number: K853756 · 1985-10-29
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Device Summary
Frequently Asked Questions
What is the DYNAMIC CARDIAC PHANTOM 74-347?
DYNAMIC CARDIAC PHANTOM 74-347 is a medical device that received FDA 510(k) clearance on 1985-10-29. The listed applicant is Victoreen, Inc.. The 510(k) number is K853756.
When did DYNAMIC CARDIAC PHANTOM 74-347 receive FDA 510(k) clearance?
DYNAMIC CARDIAC PHANTOM 74-347 received FDA 510(k) clearance on 1985-10-29, under 510(k) number K853756.
Who is the listed applicant for DYNAMIC CARDIAC PHANTOM 74-347?
The FDA 510(k) record lists Victoreen, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNAMIC CARDIAC PHANTOM 74-347?
The FDA product code for DYNAMIC CARDIAC PHANTOM 74-347 is IXY.
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 Victoreen, 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: IXY)
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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