FDA 510(k)

ADAPTER, C/D SUCTION

K-Number: K781713 · 1978-12-12

ApplicantNovametrix Medical Systems, Inc.

Decision Date1978-12-12

Product CodeBTR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

ADAPTER, C/D SUCTION 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 1978-12-12 under 510(k) number K781713. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAPTER, C/D SUCTION?

ADAPTER, C/D SUCTION is a medical device that received FDA 510(k) clearance on 1978-12-12. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K781713.

When did ADAPTER, C/D SUCTION receive FDA 510(k) clearance?

ADAPTER, C/D SUCTION received FDA 510(k) clearance on 1978-12-12, under 510(k) number K781713.

Who is the listed applicant for ADAPTER, C/D SUCTION?

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 ADAPTER, C/D SUCTION?

The FDA product code for ADAPTER, C/D SUCTION is BTR.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.