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FDA 510(k)

RESCUE VALVE

K-Number: K833748 · 1983-12-08

ApplicantRespironics, Inc.
Decision Date1983-12-08
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESCUE VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K833748. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESCUE VALVE?

RESCUE VALVE is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Respironics, Inc.. The 510(k) number is K833748.

When did RESCUE VALVE receive FDA 510(k) clearance?

RESCUE VALVE received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833748.

Who is the listed applicant for RESCUE VALVE?

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

What is the FDA product code for RESCUE VALVE?

The FDA product code for RESCUE VALVE is CBP.

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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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