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FDA 510(k)

ADIPREP ADIPOSE TRANSFER SYSTEM

K-Number: K121005 · 2012-09-21

ApplicantHarvest Technologies, Corp.
Decision Date2012-09-21
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADIPREP ADIPOSE TRANSFER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Harvest Technologies, Corp.. It received FDA 510(k) clearance on 2012-09-21 under 510(k) number K121005. 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 ADIPREP ADIPOSE TRANSFER SYSTEM?

ADIPREP ADIPOSE TRANSFER SYSTEM is a medical device that received FDA 510(k) clearance on 2012-09-21. The listed applicant is Harvest Technologies, Corp.. The 510(k) number is K121005.

When did ADIPREP ADIPOSE TRANSFER SYSTEM receive FDA 510(k) clearance?

ADIPREP ADIPOSE TRANSFER SYSTEM received FDA 510(k) clearance on 2012-09-21, under 510(k) number K121005.

Who is the listed applicant for ADIPREP ADIPOSE TRANSFER SYSTEM?

The FDA 510(k) record lists Harvest Technologies, Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADIPREP ADIPOSE TRANSFER SYSTEM?

The FDA product code for ADIPREP ADIPOSE TRANSFER SYSTEM is MUU.

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Other records listing Harvest Technologies, Corp. as applicant

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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

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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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