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FDA 510(k)

PLURIMAT;RADIOGRAPHIC TUBE MOUNT

K-Number: K781065 · 1978-07-17

Decision Date1978-07-17
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PLURIMAT;RADIOGRAPHIC TUBE MOUNT is the device name listed in this FDA 510(k) record. The listed applicant is Tecnomed, Inc.. It received FDA 510(k) clearance on 1978-07-17 under 510(k) number K781065. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 18 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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