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FDA 510(k)

HYALURONIDASE SOLUTION

K-Number: K022931 · 2002-11-04

ApplicantIrvine Scientific Sales Co., Inc.
Decision Date2002-11-04
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HYALURONIDASE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Irvine Scientific Sales Co., Inc.. It received FDA 510(k) clearance on 2002-11-04 under 510(k) number K022931. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYALURONIDASE SOLUTION?

HYALURONIDASE SOLUTION is a medical device that received FDA 510(k) clearance on 2002-11-04. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K022931.

When did HYALURONIDASE SOLUTION receive FDA 510(k) clearance?

HYALURONIDASE SOLUTION received FDA 510(k) clearance on 2002-11-04, under 510(k) number K022931.

Who is the listed applicant for HYALURONIDASE SOLUTION?

The FDA 510(k) record lists Irvine Scientific Sales Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYALURONIDASE SOLUTION?

The FDA product code for HYALURONIDASE SOLUTION is MQL.

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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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