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FDA 510(k)

SIEMENS SIRECUST 730 PATIENT MONITOR

K-Number: K890791 · 1989-05-02

Decision Date1989-05-02
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS SIRECUST 730 PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Electronics. It received FDA 510(k) clearance on 1989-05-02 under 510(k) number K890791. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SIRECUST 730 PATIENT MONITOR?

SIEMENS SIRECUST 730 PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1989-05-02. The listed applicant is Siemens Medical Electronics. The 510(k) number is K890791.

When did SIEMENS SIRECUST 730 PATIENT MONITOR receive FDA 510(k) clearance?

SIEMENS SIRECUST 730 PATIENT MONITOR received FDA 510(k) clearance on 1989-05-02, under 510(k) number K890791.

Who is the listed applicant for SIEMENS SIRECUST 730 PATIENT MONITOR?

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

What is the FDA product code for SIEMENS SIRECUST 730 PATIENT MONITOR?

The FDA product code for SIEMENS SIRECUST 730 PATIENT MONITOR is DPS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Siemens Medical Electronics as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: DPS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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