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FDA 510(k)

SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR

K-Number: K950389 · 1995-08-15

Decision Date1995-08-15
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Sorba Medical Systems, Inc.. It received FDA 510(k) clearance on 1995-08-15 under 510(k) number K950389. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR?

SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR is a medical device that received FDA 510(k) clearance on 1995-08-15. The listed applicant is Sorba Medical Systems, Inc.. The 510(k) number is K950389.

When did SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR receive FDA 510(k) clearance?

SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR received FDA 510(k) clearance on 1995-08-15, under 510(k) number K950389.

Who is the listed applicant for SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR?

The FDA 510(k) record lists Sorba Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR?

The FDA product code for SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR is DSB.

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 Sorba Medical Systems, Inc. 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.

Related Devices (Code: DSB)

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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