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FDA 510(k)

DYNAMIC CARDIAC PHANTOM 74-347

K-Number: K853756 · 1985-10-29

Decision Date1985-10-29
Product CodeIXY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DYNAMIC CARDIAC PHANTOM 74-347 is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1985-10-29 under 510(k) number K853756. The device is classified under product code IXY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 40 devices →

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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