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FDA 510(k)

POWER ASPIRATOR, MODEL LS2 OR LS2DP

K-Number: K081593 · 2008-07-23

ApplicantMedical Device Resource Corp.
Decision Date2008-07-23
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWER ASPIRATOR, MODEL LS2 OR LS2DP is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Resource Corp.. It received FDA 510(k) clearance on 2008-07-23 under 510(k) number K081593. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER ASPIRATOR, MODEL LS2 OR LS2DP?

POWER ASPIRATOR, MODEL LS2 OR LS2DP is a medical device that received FDA 510(k) clearance on 2008-07-23. The listed applicant is Medical Device Resource Corp.. The 510(k) number is K081593.

When did POWER ASPIRATOR, MODEL LS2 OR LS2DP receive FDA 510(k) clearance?

POWER ASPIRATOR, MODEL LS2 OR LS2DP received FDA 510(k) clearance on 2008-07-23, under 510(k) number K081593.

Who is the listed applicant for POWER ASPIRATOR, MODEL LS2 OR LS2DP?

The FDA 510(k) record lists Medical Device Resource Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWER ASPIRATOR, MODEL LS2 OR LS2DP?

The FDA product code for POWER ASPIRATOR, MODEL LS2 OR LS2DP is QPB.

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Other records listing Medical Device Resource Corp. as applicant

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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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