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FDA 510(k)

SIEMENS FLUID DELIVERY SYSTEM, MMT-9500

K-Number: K933545 · 1994-09-29

ApplicantSiemens Infusions Systems
Decision Date1994-09-29
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

SIEMENS FLUID DELIVERY SYSTEM, MMT-9500 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Infusions Systems. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K933545. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the SIEMENS FLUID DELIVERY SYSTEM, MMT-9500?

SIEMENS FLUID DELIVERY SYSTEM, MMT-9500 is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Siemens Infusions Systems. The 510(k) number is K933545.

When did SIEMENS FLUID DELIVERY SYSTEM, MMT-9500 receive FDA 510(k) clearance?

SIEMENS FLUID DELIVERY SYSTEM, MMT-9500 received FDA 510(k) clearance on 1994-09-29, under 510(k) number K933545.

Who is the listed applicant for SIEMENS FLUID DELIVERY SYSTEM, MMT-9500?

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

What is the FDA product code for SIEMENS FLUID DELIVERY SYSTEM, MMT-9500?

The FDA product code for SIEMENS FLUID DELIVERY SYSTEM, MMT-9500 is FRN.

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Official Source

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

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