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)

LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE

K-Number: K121703 · 2012-12-07

Decision Date2012-12-07
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Khan USA, Inc.. It received FDA 510(k) clearance on 2012-12-07 under 510(k) number K121703. 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 LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE?

LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE is a medical device that received FDA 510(k) clearance on 2012-12-07. The listed applicant is Medi-Khan USA, Inc.. The 510(k) number is K121703.

When did LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE receive FDA 510(k) clearance?

LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE received FDA 510(k) clearance on 2012-12-07, under 510(k) number K121703.

Who is the listed applicant for LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE?

The FDA 510(k) record lists Medi-Khan USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE?

The FDA product code for LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE 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.

Other records listing Medi-Khan USA, 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.

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.

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.

↑