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FDA 510(k)

RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE

K-Number: K934699 · 1995-01-05

ApplicantRespironics, Inc.
Decision Date1995-01-05
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1995-01-05 under 510(k) number K934699. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE?

RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE is a medical device that received FDA 510(k) clearance on 1995-01-05. The listed applicant is Respironics, Inc.. The 510(k) number is K934699.

When did RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE receive FDA 510(k) clearance?

RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE received FDA 510(k) clearance on 1995-01-05, under 510(k) number K934699.

Who is the listed applicant for RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE?

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 BAGEASY ENCOR ADULT SEMI-REUSABLE?

The FDA product code for RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE is BTM.

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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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