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FDA 510(k)

SIREMOBIL COMPACT

K-Number: K963093 · 1996-09-03

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1996-09-03
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIREMOBIL COMPACT 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 1996-09-03 under 510(k) number K963093. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIREMOBIL COMPACT?

SIREMOBIL COMPACT is a medical device that received FDA 510(k) clearance on 1996-09-03. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K963093.

When did SIREMOBIL COMPACT receive FDA 510(k) clearance?

SIREMOBIL COMPACT received FDA 510(k) clearance on 1996-09-03, under 510(k) number K963093.

Who is the listed applicant for SIREMOBIL COMPACT?

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 SIREMOBIL COMPACT?

The FDA product code for SIREMOBIL COMPACT is OXO.

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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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