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FDA 510(k)

MODEL RS-3 RADIOGRAPHIC STAND

K-Number: K861995 · 1986-06-19

Decision Date1986-06-19
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL RS-3 RADIOGRAPHIC STAND is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1986-06-19 under 510(k) number K861995. 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 MODEL RS-3 RADIOGRAPHIC STAND?

MODEL RS-3 RADIOGRAPHIC STAND is a medical device that received FDA 510(k) clearance on 1986-06-19. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K861995.

When did MODEL RS-3 RADIOGRAPHIC STAND receive FDA 510(k) clearance?

MODEL RS-3 RADIOGRAPHIC STAND received FDA 510(k) clearance on 1986-06-19, under 510(k) number K861995.

Who is the listed applicant for MODEL RS-3 RADIOGRAPHIC STAND?

The FDA 510(k) record lists Medicor USA , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL RS-3 RADIOGRAPHIC STAND?

The FDA product code for MODEL RS-3 RADIOGRAPHIC STAND 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 Medicor USA , Ltd. 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 14 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

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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