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FDA 510(k)

RESPIRONICS REMSTAR WITH REMOTE AND RAMP

K-Number: K911856 · 1991-08-09

ApplicantRespironics, Inc.
Decision Date1991-08-09
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRONICS REMSTAR WITH REMOTE AND RAMP is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1991-08-09 under 510(k) number K911856. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRONICS REMSTAR WITH REMOTE AND RAMP?

RESPIRONICS REMSTAR WITH REMOTE AND RAMP is a medical device that received FDA 510(k) clearance on 1991-08-09. The listed applicant is Respironics, Inc.. The 510(k) number is K911856.

When did RESPIRONICS REMSTAR WITH REMOTE AND RAMP receive FDA 510(k) clearance?

RESPIRONICS REMSTAR WITH REMOTE AND RAMP received FDA 510(k) clearance on 1991-08-09, under 510(k) number K911856.

Who is the listed applicant for RESPIRONICS REMSTAR WITH REMOTE AND RAMP?

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 REMSTAR WITH REMOTE AND RAMP?

The FDA product code for RESPIRONICS REMSTAR WITH REMOTE AND RAMP is BZD.

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Related Devices (Code: BZD)

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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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