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FDA 510(k)

INFRARED EXPOSURE HAND SWITCH

K-Number: K930049 · 1993-06-22

Decision Date1993-06-22
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INFRARED EXPOSURE HAND SWITCH is the device name listed in this FDA 510(k) record. The listed applicant is Mid X-Ray, Inc.. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K930049. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFRARED EXPOSURE HAND SWITCH?

INFRARED EXPOSURE HAND SWITCH is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Mid X-Ray, Inc.. The 510(k) number is K930049.

When did INFRARED EXPOSURE HAND SWITCH receive FDA 510(k) clearance?

INFRARED EXPOSURE HAND SWITCH received FDA 510(k) clearance on 1993-06-22, under 510(k) number K930049.

Who is the listed applicant for INFRARED EXPOSURE HAND SWITCH?

The FDA 510(k) record lists Mid X-Ray, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INFRARED EXPOSURE HAND SWITCH?

The FDA product code for INFRARED EXPOSURE HAND SWITCH is IZL.

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: IZL)

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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