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FDA 510(k)

RESPIRONICS PR VALVE

K-Number: K833327 · 1983-11-28

ApplicantRespironics, Inc.
Decision Date1983-11-28
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRONICS PR 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 1983-11-28 under 510(k) number K833327. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRONICS PR VALVE?

RESPIRONICS PR VALVE is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Respironics, Inc.. The 510(k) number is K833327.

When did RESPIRONICS PR VALVE receive FDA 510(k) clearance?

RESPIRONICS PR VALVE received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833327.

Who is the listed applicant for RESPIRONICS PR 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 RESPIRONICS PR VALVE?

The FDA product code for RESPIRONICS PR VALVE is BSK.

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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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