BLASTFREEZE AND BLASTTHAW
K-Number: K031486 · 2003-06-27
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Device Summary
Frequently Asked Questions
What is the BLASTFREEZE AND BLASTTHAW?
BLASTFREEZE AND BLASTTHAW is a medical device that received FDA 510(k) clearance on 2003-06-27. The listed applicant is Medicult A/S. The 510(k) number is K031486.
When did BLASTFREEZE AND BLASTTHAW receive FDA 510(k) clearance?
BLASTFREEZE AND BLASTTHAW received FDA 510(k) clearance on 2003-06-27, under 510(k) number K031486.
Who is the listed applicant for BLASTFREEZE AND BLASTTHAW?
The FDA 510(k) record lists Medicult A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLASTFREEZE AND BLASTTHAW?
The FDA product code for BLASTFREEZE AND BLASTTHAW 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 Medicult A/S 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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