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FDA 510(k)

SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL

K-Number: K003243 · 2000-12-21

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2000-12-21
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL 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 2000-12-21 under 510(k) number K003243. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL?

SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL is a medical device that received FDA 510(k) clearance on 2000-12-21. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K003243.

When did SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL receive FDA 510(k) clearance?

SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL received FDA 510(k) clearance on 2000-12-21, under 510(k) number K003243.

Who is the listed applicant for SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL?

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 SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL?

The FDA product code for SIEMENS INFINITY MODULAR MONITORS MODEL SC 8000; SC 7000; SC 9000XL is MHX.

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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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