FDA 510(k)

SIZE SENSING CASSETTE TRAY

K-Number: K827504 · 1982-06-09

Decision Date1982-06-09

Product Code

DecisionSubstantially Equivalent

Device Summary

SIZE SENSING CASSETTE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Midwest X-Ray Equipment Co.. It received FDA 510(k) clearance on 1982-06-09 under 510(k) number K827504. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIZE SENSING CASSETTE TRAY?

SIZE SENSING CASSETTE TRAY is a medical device that received FDA 510(k) clearance on 1982-06-09. The listed applicant is Midwest X-Ray Equipment Co.. The 510(k) number is K827504.

When did SIZE SENSING CASSETTE TRAY receive FDA 510(k) clearance?

SIZE SENSING CASSETTE TRAY received FDA 510(k) clearance on 1982-06-09, under 510(k) number K827504.

Who is the listed applicant for SIZE SENSING CASSETTE TRAY?

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

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.

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Other records listing Midwest X-Ray Equipment Co. as applicant

K924423MWX-7440 HIGH SPEED BUCKY K827609MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY

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.