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FDA 510(k)

LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200

K-Number: K092284 · 2009-09-01

ApplicantMedical Device Resource Corp.
Decision Date2009-09-01
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200 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 2009-09-01 under 510(k) number K092284. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200?

LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200 is a medical device that received FDA 510(k) clearance on 2009-09-01. The listed applicant is Medical Device Resource Corp.. The 510(k) number is K092284.

When did LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200 receive FDA 510(k) clearance?

LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200 received FDA 510(k) clearance on 2009-09-01, under 510(k) number K092284.

Who is the listed applicant for LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200?

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 LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200?

The FDA product code for LIPISYSTEMS AQUAVAGE, MODELS AV2000 AND AV1200 is MUU.

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Other records listing Medical Device Resource Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K081593POWER ASPIRATOR, MODEL LS2 OR LS2DP

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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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