FDA 510(k)

ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR

K-Number: K790312 · 1979-02-21

ApplicantRespiratory Support Products, Inc.

Decision Date1979-02-21

Product CodeBTR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Support Products, Inc.. It received FDA 510(k) clearance on 1979-02-21 under 510(k) number K790312. 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 ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR?

ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR is a medical device that received FDA 510(k) clearance on 1979-02-21. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K790312.

When did ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR receive FDA 510(k) clearance?

ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR received FDA 510(k) clearance on 1979-02-21, under 510(k) number K790312.

Who is the listed applicant for ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR?

The FDA 510(k) record lists Respiratory Support Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR?

The FDA product code for ENDOTRACHEAL TUBE W/HOLDER & CONNECTOR is BTR.

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Related Devices (Code: BTR)

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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.