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FDA 510(k)

POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS

K-Number: K837354 · 1983-04-21

ApplicantGeneral Electric Co.
Decision Date1983-04-21
Product Code
DecisionSubstantially Equivalent

Device Summary

POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1983-04-21 under 510(k) number K837354. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS?

POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS is a medical device that received FDA 510(k) clearance on 1983-04-21. The listed applicant is General Electric Co.. The 510(k) number is K837354.

When did POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS receive FDA 510(k) clearance?

POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS received FDA 510(k) clearance on 1983-04-21, under 510(k) number K837354.

Who is the listed applicant for POWERED MOBILE BASE FOR 200MM AND 300MM SIZE DETECTORS?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing General Electric Co. as applicant

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Official Source

View on FDA Database →

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

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