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FDA 510(k)

ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810

K-Number: K062144 · 2006-10-12

ApplicantInvivo Corporation
Decision Date2006-10-12
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810 is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation. It received FDA 510(k) clearance on 2006-10-12 under 510(k) number K062144. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810?

ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810 is a medical device that received FDA 510(k) clearance on 2006-10-12. The listed applicant is Invivo Corporation. The 510(k) number is K062144.

When did ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810 receive FDA 510(k) clearance?

ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810 received FDA 510(k) clearance on 2006-10-12, under 510(k) number K062144.

Who is the listed applicant for ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810?

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

What is the FDA product code for ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810?

The FDA product code for ESCORT M8 VITAL SIGNS PATIENT MONITOR, MODEL 3810 is MHX.

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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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