PLURIMAT;RADIOGRAPHIC TUBE MOUNT
K-Number: K781065 · 1978-07-17
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Device Summary
Frequently Asked Questions
What is the PLURIMAT;RADIOGRAPHIC TUBE MOUNT?
PLURIMAT;RADIOGRAPHIC TUBE MOUNT is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Tecnomed, Inc.. The 510(k) number is K781065.
When did PLURIMAT;RADIOGRAPHIC TUBE MOUNT receive FDA 510(k) clearance?
PLURIMAT;RADIOGRAPHIC TUBE MOUNT received FDA 510(k) clearance on 1978-07-17, under 510(k) number K781065.
Who is the listed applicant for PLURIMAT;RADIOGRAPHIC TUBE MOUNT?
The FDA 510(k) record lists Tecnomed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLURIMAT;RADIOGRAPHIC TUBE MOUNT?
The FDA product code for PLURIMAT;RADIOGRAPHIC TUBE MOUNT is IYB.
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 Tecnomed, 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: IYB)
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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