Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SOYEE ALUMINUM INTERSPACED X-RAY GRID

K-Number: K926445 · 1993-04-07

Decision Date1993-04-07
Product CodeIXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOYEE ALUMINUM INTERSPACED X-RAY GRID is the device name listed in this FDA 510(k) record. The listed applicant is X-Ray Accessories Mfg. Co.. It received FDA 510(k) clearance on 1993-04-07 under 510(k) number K926445. 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 SOYEE ALUMINUM INTERSPACED X-RAY GRID?

SOYEE ALUMINUM INTERSPACED X-RAY GRID is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is X-Ray Accessories Mfg. Co.. The 510(k) number is K926445.

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

SOYEE ALUMINUM INTERSPACED X-RAY GRID received FDA 510(k) clearance on 1993-04-07, under 510(k) number K926445.

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

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

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

The FDA product code for SOYEE 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 X-Ray Accessories Mfg. 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.

↑