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FDA 510(k)

CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP

K-Number: K931133 · 1995-03-29

Decision Date1995-03-29
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP is the device name listed in this FDA 510(k) record. The listed applicant is Clinicomp, Inc.. It received FDA 510(k) clearance on 1995-03-29 under 510(k) number K931133. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP?

CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP is a medical device that received FDA 510(k) clearance on 1995-03-29. The listed applicant is Clinicomp, Inc.. The 510(k) number is K931133.

When did CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP receive FDA 510(k) clearance?

CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP received FDA 510(k) clearance on 1995-03-29, under 510(k) number K931133.

Who is the listed applicant for CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP?

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

What is the FDA product code for CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP?

The FDA product code for CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP is HGM.

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 Clinicomp, 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: HGM)

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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