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FDA 510(k)

MEDELA DOMINANT 50 LIPO, MODEL 600-5706

K-Number: K063336 · 2007-02-26

ApplicantMedela AG
Decision Date2007-02-26
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDELA DOMINANT 50 LIPO, MODEL 600-5706 is the device name listed in this FDA 510(k) record. The listed applicant is Medela AG. It received FDA 510(k) clearance on 2007-02-26 under 510(k) number K063336. 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 MEDELA DOMINANT 50 LIPO, MODEL 600-5706?

MEDELA DOMINANT 50 LIPO, MODEL 600-5706 is a medical device that received FDA 510(k) clearance on 2007-02-26. The listed applicant is Medela AG. The 510(k) number is K063336.

When did MEDELA DOMINANT 50 LIPO, MODEL 600-5706 receive FDA 510(k) clearance?

MEDELA DOMINANT 50 LIPO, MODEL 600-5706 received FDA 510(k) clearance on 2007-02-26, under 510(k) number K063336.

Who is the listed applicant for MEDELA DOMINANT 50 LIPO, MODEL 600-5706?

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

What is the FDA product code for MEDELA DOMINANT 50 LIPO, MODEL 600-5706?

The FDA product code for MEDELA DOMINANT 50 LIPO, MODEL 600-5706 is QPB.

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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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