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FDA 510(k)

MOBILETTE XP AND MOBILETT XPHYBRID

K-Number: K033238 · 2003-11-14

ApplicantSiemens Medical Systems, Inc.
Decision Date2003-11-14
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILETTE XP AND MOBILETT XPHYBRID is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Systems, Inc.. It received FDA 510(k) clearance on 2003-11-14 under 510(k) number K033238. 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 MOBILETTE XP AND MOBILETT XPHYBRID?

MOBILETTE XP AND MOBILETT XPHYBRID is a medical device that received FDA 510(k) clearance on 2003-11-14. The listed applicant is Siemens Medical Systems, Inc.. The 510(k) number is K033238.

When did MOBILETTE XP AND MOBILETT XPHYBRID receive FDA 510(k) clearance?

MOBILETTE XP AND MOBILETT XPHYBRID received FDA 510(k) clearance on 2003-11-14, under 510(k) number K033238.

Who is the listed applicant for MOBILETTE XP AND MOBILETT XPHYBRID?

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

What is the FDA product code for MOBILETTE XP AND MOBILETT XPHYBRID?

The FDA product code for MOBILETTE XP AND MOBILETT XPHYBRID 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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