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FDA 510(k)

MOBILETT PLUS MOBILE X-RAY SYSTEM

K-Number: K932106 · 1994-09-14

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-09-14
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILETT PLUS MOBILE X-RAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1994-09-14 under 510(k) number K932106. 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 MOBILETT PLUS MOBILE X-RAY SYSTEM?

MOBILETT PLUS MOBILE X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K932106.

When did MOBILETT PLUS MOBILE X-RAY SYSTEM receive FDA 510(k) clearance?

MOBILETT PLUS MOBILE X-RAY SYSTEM received FDA 510(k) clearance on 1994-09-14, under 510(k) number K932106.

Who is the listed applicant for MOBILETT PLUS MOBILE X-RAY SYSTEM?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOBILETT PLUS MOBILE X-RAY SYSTEM?

The FDA product code for MOBILETT PLUS MOBILE X-RAY SYSTEM is IZL.

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Related Devices (Code: IZL)

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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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