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FDA 510(k)

MD TURBO

K-Number: K051284 · 2005-06-22

ApplicantRespirics, Inc.
Decision Date2005-06-22
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MD TURBO is the device name listed in this FDA 510(k) record. The listed applicant is Respirics, Inc.. It received FDA 510(k) clearance on 2005-06-22 under 510(k) number K051284. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MD TURBO?

MD TURBO is a medical device that received FDA 510(k) clearance on 2005-06-22. The listed applicant is Respirics, Inc.. The 510(k) number is K051284.

When did MD TURBO receive FDA 510(k) clearance?

MD TURBO received FDA 510(k) clearance on 2005-06-22, under 510(k) number K051284.

Who is the listed applicant for MD TURBO?

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

What is the FDA product code for MD TURBO?

The FDA product code for MD TURBO is CAF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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