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FDA 510(k)

BIPAP MODEL S/T-D

K-Number: K951264 · 1996-07-29

ApplicantRespironics, Inc.
Decision Date1996-07-29
Product CodeMNT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BIPAP MODEL S/T-D is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1996-07-29 under 510(k) number K951264. The device is classified under product code MNT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIPAP MODEL S/T-D?

BIPAP MODEL S/T-D is a medical device that received FDA 510(k) clearance on 1996-07-29. The listed applicant is Respironics, Inc.. The 510(k) number is K951264.

When did BIPAP MODEL S/T-D receive FDA 510(k) clearance?

BIPAP MODEL S/T-D received FDA 510(k) clearance on 1996-07-29, under 510(k) number K951264.

Who is the listed applicant for BIPAP MODEL S/T-D?

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 BIPAP MODEL S/T-D?

The FDA product code for BIPAP MODEL S/T-D is MNT.

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Related Devices (Code: MNT)

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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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