MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902
K-Number: K860100 · 1986-04-22
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Device Summary
Frequently Asked Questions
What is the MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902?
MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902 is a medical device that received FDA 510(k) clearance on 1986-04-22. The listed applicant is Victoreen, Inc.. The 510(k) number is K860100.
When did MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902 receive FDA 510(k) clearance?
MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902 received FDA 510(k) clearance on 1986-04-22, under 510(k) number K860100.
Who is the listed applicant for MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902?
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 MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902?
The FDA product code for MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902 is LHO.
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: LHO)
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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