JPI ALUMINUM INTERSPACED X-RAY GRID
K-Number: K926261 · 1993-03-18
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Device Summary
Frequently Asked Questions
What is the JPI ALUMINUM INTERSPACED X-RAY GRID?
JPI ALUMINUM INTERSPACED X-RAY GRID is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is Jpi, Inc.. The 510(k) number is K926261.
When did JPI ALUMINUM INTERSPACED X-RAY GRID receive FDA 510(k) clearance?
JPI ALUMINUM INTERSPACED X-RAY GRID received FDA 510(k) clearance on 1993-03-18, under 510(k) number K926261.
Who is the listed applicant for JPI ALUMINUM INTERSPACED X-RAY GRID?
The FDA 510(k) record lists Jpi, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JPI ALUMINUM INTERSPACED X-RAY GRID?
The FDA product code for JPI 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.
Other records listing Jpi, 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: 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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