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FDA 510(k)

MODIFIED HAM'S F-10 WITH ALBUMIN

K-Number: K991420 · 1999-07-02

Decision Date1999-07-02
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODIFIED HAM'S F-10 WITH ALBUMIN 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 1999-07-02 under 510(k) number K991420. 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 MODIFIED HAM'S F-10 WITH ALBUMIN?

MODIFIED HAM'S F-10 WITH ALBUMIN is a medical device that received FDA 510(k) clearance on 1999-07-02. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K991420.

When did MODIFIED HAM'S F-10 WITH ALBUMIN receive FDA 510(k) clearance?

MODIFIED HAM'S F-10 WITH ALBUMIN received FDA 510(k) clearance on 1999-07-02, under 510(k) number K991420.

Who is the listed applicant for MODIFIED HAM'S F-10 WITH ALBUMIN?

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 MODIFIED HAM'S F-10 WITH ALBUMIN?

The FDA product code for MODIFIED HAM'S F-10 WITH ALBUMIN is MQL.

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 Irvine Scientific Sales Co., 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.

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Related Devices (Code: MQL)

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

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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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