Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIPCOLLECTOR II

K-Number: K101713 · 2010-06-29

ApplicantHuman Med AG
Decision Date2010-06-29
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIPCOLLECTOR II is the device name listed in this FDA 510(k) record. The listed applicant is Human Med AG. It received FDA 510(k) clearance on 2010-06-29 under 510(k) number K101713. 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 LIPCOLLECTOR II?

LIPCOLLECTOR II is a medical device that received FDA 510(k) clearance on 2010-06-29. The listed applicant is Human Med AG. The 510(k) number is K101713.

When did LIPCOLLECTOR II receive FDA 510(k) clearance?

LIPCOLLECTOR II received FDA 510(k) clearance on 2010-06-29, under 510(k) number K101713.

Who is the listed applicant for LIPCOLLECTOR II?

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

What is the FDA product code for LIPCOLLECTOR II?

The FDA product code for LIPCOLLECTOR II is MUU.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Human Med AG 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.

K082025BODY-JET

Related Devices (Code: MUU)

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.

K210528IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) KitMillennium Medical Technologies Inc (Dba Cellmyx)K203800SyntrFuge SystemSyntr Health Technologies, Inc.K202443Smart Kit Basic, Smart Kit ProBsl Co., Ltd.K193539REVOLVE ENVI 600 Advanced Adipose SystemLifecell CorporationK193363Dermapose RefreshPuregraft, LLCK182732JTL-250-01Jointechlabs, Inc.

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.

↑