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FDA 510(k)

VENTRAK RMMS 1550

K-Number: K960831 · 1996-05-29

ApplicantNovametrix Medical Systems, Inc.
Decision Date1996-05-29
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTRAK RMMS 1550 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 1996-05-29 under 510(k) number K960831. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTRAK RMMS 1550?

VENTRAK RMMS 1550 is a medical device that received FDA 510(k) clearance on 1996-05-29. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K960831.

When did VENTRAK RMMS 1550 receive FDA 510(k) clearance?

VENTRAK RMMS 1550 received FDA 510(k) clearance on 1996-05-29, under 510(k) number K960831.

Who is the listed applicant for VENTRAK RMMS 1550?

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 VENTRAK RMMS 1550?

The FDA product code for VENTRAK RMMS 1550 is BZC.

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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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