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)

Vitruvian Liposaber

K-Number: K240188 · 2024-09-13

ApplicantBlack & Black Surgical, Inc.
Decision Date2024-09-13
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vitruvian Liposaber is the device name listed in this FDA 510(k) record. The listed applicant is Black & Black Surgical, Inc.. It received FDA 510(k) clearance on 2024-09-13 under 510(k) number K240188. 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 Vitruvian Liposaber?

Vitruvian Liposaber is a medical device that received FDA 510(k) clearance on 2024-09-13. The listed applicant is Black & Black Surgical, Inc.. The 510(k) number is K240188.

When did Vitruvian Liposaber receive FDA 510(k) clearance?

Vitruvian Liposaber received FDA 510(k) clearance on 2024-09-13, under 510(k) number K240188.

Who is the listed applicant for Vitruvian Liposaber?

The FDA 510(k) record lists Black & Black Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vitruvian Liposaber?

The FDA product code for Vitruvian Liposaber is QPB.

Other records listing Black & Black Surgical, Inc. 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.

K170629VITRUVIAN INFILTRATION PUMPK161722VITRUVIAN ULTIMATE ASPIRATOR

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.

K251944Lipocosm Harmonic SystemLipocosm, LLCK253396AYON Body Contouring System™ (AYON SYSTEM)Apyx Medical CorporationK252495LSSA (NP-200)Newpong Co., Ltd.K244050AYON Body Contouring System (AYON SYSTEM)Apyx Medical CorporationK244026PAL 7020 ConsoleMicroaire Surgical Instruments, LLCK242804PAL Aspiration SystemMicroaire Surgical Instruments, LLC

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.

↑