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FDA 510(k)

INFRARED EXPOSURE HAND SWITCH

K-Number: K950442 · 1995-03-31

ApplicantMedical X-Ray Intl., Inc.
Decision Date1995-03-31
Product CodeKXJ
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 Medical X-Ray Intl., Inc.. It received FDA 510(k) clearance on 1995-03-31 under 510(k) number K950442. The device is classified under product code KXJ. 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 1995-03-31. The listed applicant is Medical X-Ray Intl., Inc.. The 510(k) number is K950442.

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

INFRARED EXPOSURE HAND SWITCH received FDA 510(k) clearance on 1995-03-31, under 510(k) number K950442.

Who is the listed applicant for INFRARED EXPOSURE HAND SWITCH?

The FDA 510(k) record lists Medical X-Ray Intl., 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 KXJ.

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Related Devices (Code: KXJ)

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.

K050190APOLLOVilla Sistemi Medicali S.P.A.K963905RADIOGRAPHIC ITT TABLEX-Ray Technologies, Inc.K955414XRT 400Wuestec Medical, Inc.K951146IMAGING TABLESepta Corp.K950068CARBON FIBER COUCH INSERTMedtec, Inc.K940696SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5Philips Medical Systems North America, Inc.

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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