VIT KIT - FREEZE AND THAW
K-Number: K093273 · 2010-03-03
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Device Summary
Frequently Asked Questions
What is the VIT KIT - FREEZE AND THAW?
VIT KIT - FREEZE AND THAW is a medical device that received FDA 510(k) clearance on 2010-03-03. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K093273.
When did VIT KIT - FREEZE AND THAW receive FDA 510(k) clearance?
VIT KIT - FREEZE AND THAW received FDA 510(k) clearance on 2010-03-03, under 510(k) number K093273.
Who is the listed applicant for VIT KIT - FREEZE AND THAW?
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 VIT KIT - FREEZE AND THAW?
The FDA product code for VIT KIT - FREEZE AND THAW 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.
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
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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