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FDA 510(k)

MITAYA ALUMINUM INTERSPACED X-RAY GRID

K-Number: K964025 · 1997-06-13

Decision Date1997-06-13
Product CodeIXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MITAYA ALUMINUM INTERSPACED X-RAY GRID is the device name listed in this FDA 510(k) record. The listed applicant is X-Ray Accessory Corp.. It received FDA 510(k) clearance on 1997-06-13 under 510(k) number K964025. The device is classified under product code IXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MITAYA ALUMINUM INTERSPACED X-RAY GRID?

MITAYA ALUMINUM INTERSPACED X-RAY GRID is a medical device that received FDA 510(k) clearance on 1997-06-13. The listed applicant is X-Ray Accessory Corp.. The 510(k) number is K964025.

When did MITAYA ALUMINUM INTERSPACED X-RAY GRID receive FDA 510(k) clearance?

MITAYA ALUMINUM INTERSPACED X-RAY GRID received FDA 510(k) clearance on 1997-06-13, under 510(k) number K964025.

Who is the listed applicant for MITAYA ALUMINUM INTERSPACED X-RAY GRID?

The FDA 510(k) record lists X-Ray Accessory Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MITAYA ALUMINUM INTERSPACED X-RAY GRID?

The FDA product code for MITAYA ALUMINUM INTERSPACED X-RAY GRID is IXJ.

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.

Related Devices (Code: IXJ)

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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