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FDA 510(k)

OMNI-CENTRAL STATION MONITOR

K-Number: K936051 · 1994-07-06

ApplicantInvivo Research, Inc.
Decision Date1994-07-06
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OMNI-CENTRAL STATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Research, Inc.. It received FDA 510(k) clearance on 1994-07-06 under 510(k) number K936051. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNI-CENTRAL STATION MONITOR?

OMNI-CENTRAL STATION MONITOR is a medical device that received FDA 510(k) clearance on 1994-07-06. The listed applicant is Invivo Research, Inc.. The 510(k) number is K936051.

When did OMNI-CENTRAL STATION MONITOR receive FDA 510(k) clearance?

OMNI-CENTRAL STATION MONITOR received FDA 510(k) clearance on 1994-07-06, under 510(k) number K936051.

Who is the listed applicant for OMNI-CENTRAL STATION MONITOR?

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

What is the FDA product code for OMNI-CENTRAL STATION MONITOR?

The FDA product code for OMNI-CENTRAL STATION MONITOR is DRT.

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Other records listing Invivo Research, Inc. as applicant

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Related Devices (Code: DRT)

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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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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