FDA 510(k)

X RAY TUBE HOUSING/INSERT

K-Number: K837111 · 1983-03-09

Decision Date1983-03-09

Product Code

DecisionSubstantially Equivalent

Device Summary

X RAY TUBE HOUSING/INSERT is the device name listed in this FDA 510(k) record. The listed applicant is Atlantic Imaging Corp.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K837111. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X RAY TUBE HOUSING/INSERT?

X RAY TUBE HOUSING/INSERT is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Atlantic Imaging Corp.. The 510(k) number is K837111.

When did X RAY TUBE HOUSING/INSERT receive FDA 510(k) clearance?

X RAY TUBE HOUSING/INSERT received FDA 510(k) clearance on 1983-03-09, under 510(k) number K837111.

Who is the listed applicant for X RAY TUBE HOUSING/INSERT?

The FDA 510(k) record lists Atlantic Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.

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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.