MITAYA ALUMINUM INTERSPACED X-RAY GRID
K-Number: K964025 · 1997-06-13
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Device Summary
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
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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