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FDA 510(k)

NOVAMETRIX PHYSIOLOGICAL MONITOR #910

K-Number: K811893 · 1981-09-08

ApplicantNovametrix Medical Systems, Inc.
Decision Date1981-09-08
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NOVAMETRIX PHYSIOLOGICAL MONITOR #910 is the device name listed in this FDA 510(k) record. The listed applicant is Novametrix Medical Systems, Inc.. It received FDA 510(k) clearance on 1981-09-08 under 510(k) number K811893. 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 NOVAMETRIX PHYSIOLOGICAL MONITOR #910?

NOVAMETRIX PHYSIOLOGICAL MONITOR #910 is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K811893.

When did NOVAMETRIX PHYSIOLOGICAL MONITOR #910 receive FDA 510(k) clearance?

NOVAMETRIX PHYSIOLOGICAL MONITOR #910 received FDA 510(k) clearance on 1981-09-08, under 510(k) number K811893.

Who is the listed applicant for NOVAMETRIX PHYSIOLOGICAL MONITOR #910?

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

What is the FDA product code for NOVAMETRIX PHYSIOLOGICAL MONITOR #910?

The FDA product code for NOVAMETRIX PHYSIOLOGICAL MONITOR #910 is DRT.

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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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