FDA 510(k)

ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE

K-Number: K854632 · 1986-01-03

ApplicantRespiratory Support Products, Inc.

Decision Date1986-01-03

Product CodeBTR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE 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 1986-01-03 under 510(k) number K854632. 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 GUIDE OR INTUBATION STYLETTE?

ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE is a medical device that received FDA 510(k) clearance on 1986-01-03. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K854632.

When did ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE receive FDA 510(k) clearance?

ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE received FDA 510(k) clearance on 1986-01-03, under 510(k) number K854632.

Who is the listed applicant for ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE?

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 GUIDE OR INTUBATION STYLETTE?

The FDA product code for ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE is 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.