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FDA 510(k)

NOVAMETRIX MODEL 200 MAGSTIM

K-Number: K871338 · 1987-08-04

ApplicantNovametrix Medical Systems, Inc.
Decision Date1987-08-04
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NOVAMETRIX MODEL 200 MAGSTIM 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 1987-08-04 under 510(k) number K871338. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVAMETRIX MODEL 200 MAGSTIM?

NOVAMETRIX MODEL 200 MAGSTIM is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K871338.

When did NOVAMETRIX MODEL 200 MAGSTIM receive FDA 510(k) clearance?

NOVAMETRIX MODEL 200 MAGSTIM received FDA 510(k) clearance on 1987-08-04, under 510(k) number K871338.

Who is the listed applicant for NOVAMETRIX MODEL 200 MAGSTIM?

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 MODEL 200 MAGSTIM?

The FDA product code for NOVAMETRIX MODEL 200 MAGSTIM is GWF.

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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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