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FDA 510(k)

ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE

K-Number: K942190 · 1994-08-17

Decision Date1994-08-17
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Image Diagnostics, Inc.. It received FDA 510(k) clearance on 1994-08-17 under 510(k) number K942190. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE?

ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Image Diagnostics, Inc.. The 510(k) number is K942190.

When did ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE receive FDA 510(k) clearance?

ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE received FDA 510(k) clearance on 1994-08-17, under 510(k) number K942190.

Who is the listed applicant for ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE?

The FDA 510(k) record lists Image Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE?

The FDA product code for ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE is IXQ.

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 Image Diagnostics, 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: IXQ)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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