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FDA 510(k)

SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960)

K-Number: K952054 · 1996-06-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1996-06-07
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960) 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 1996-06-07 under 510(k) number K952054. 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 MONITORING (1200, 1200 NEO, 960)?

SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960) is a medical device that received FDA 510(k) clearance on 1996-06-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K952054.

When did SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960) receive FDA 510(k) clearance?

SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960) received FDA 510(k) clearance on 1996-06-07, under 510(k) number K952054.

Who is the listed applicant for SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960)?

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 MONITORING (1200, 1200 NEO, 960)?

The FDA product code for SIEMENS SIRECUST MONITORING (1200, 1200 NEO, 960) 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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