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FDA 510(k)

LIPOSOL

K-Number: K830472 · 1983-06-08

ApplicantQuest Medical, Inc.
Decision Date1983-06-08
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIPOSOL is the device name listed in this FDA 510(k) record. The listed applicant is Quest Medical, Inc.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K830472. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIPOSOL?

LIPOSOL is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Quest Medical, Inc.. The 510(k) number is K830472.

When did LIPOSOL receive FDA 510(k) clearance?

LIPOSOL received FDA 510(k) clearance on 1983-06-08, under 510(k) number K830472.

Who is the listed applicant for LIPOSOL?

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

What is the FDA product code for LIPOSOL?

The FDA product code for LIPOSOL is JKA.

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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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