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FDA 510(k)

SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS

K-Number: K933177 · 1995-04-10

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-04-10
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS 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 1995-04-10 under 510(k) number K933177. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS?

SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS is a medical device that received FDA 510(k) clearance on 1995-04-10. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K933177.

When did SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS receive FDA 510(k) clearance?

SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS received FDA 510(k) clearance on 1995-04-10, under 510(k) number K933177.

Who is the listed applicant for SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS?

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 SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS?

The FDA product code for SIEMENS SIRECUST 700 BEDSIDE MONITOR MODIFICATIONS is DSI.

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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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