LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688
K-Number: K072793 · 2008-03-04
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Device Summary
Frequently Asked Questions
What is the LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688?
LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688 is a medical device that received FDA 510(k) clearance on 2008-03-04. The listed applicant is Moeller Medical GmbH & Co. KG. The 510(k) number is K072793.
When did LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688 receive FDA 510(k) clearance?
LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688 received FDA 510(k) clearance on 2008-03-04, under 510(k) number K072793.
Who is the listed applicant for LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688?
The FDA 510(k) record lists Moeller Medical GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688?
The FDA product code for LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688 is QPB.
Related Clinical Trials
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.
Other records listing Moeller Medical GmbH & Co. KG 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.
Related Devices (Code: QPB)
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.
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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