X-RAY GRID (RADIOLOGICAL GRID)
K-Number: K940309 · 1994-04-22
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Device Summary
Frequently Asked Questions
What is the X-RAY GRID (RADIOLOGICAL GRID)?
X-RAY GRID (RADIOLOGICAL GRID) is a medical device that received FDA 510(k) clearance on 1994-04-22. The listed applicant is J.P.I. Chicago Co.. The 510(k) number is K940309.
When did X-RAY GRID (RADIOLOGICAL GRID) receive FDA 510(k) clearance?
X-RAY GRID (RADIOLOGICAL GRID) received FDA 510(k) clearance on 1994-04-22, under 510(k) number K940309.
Who is the listed applicant for X-RAY GRID (RADIOLOGICAL GRID)?
The FDA 510(k) record lists J.P.I. Chicago Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-RAY GRID (RADIOLOGICAL GRID)?
The FDA product code for X-RAY GRID (RADIOLOGICAL 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 J.P.I. Chicago Co. 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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