HSA-SOLUTION, MODEL 10034/10064
K-Number: K021896 · 2002-09-06
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Device Summary
Frequently Asked Questions
What is the HSA-SOLUTION, MODEL 10034/10064?
HSA-SOLUTION, MODEL 10034/10064 is a medical device that received FDA 510(k) clearance on 2002-09-06. The listed applicant is Vitrolife Sweden AB. The 510(k) number is K021896.
When did HSA-SOLUTION, MODEL 10034/10064 receive FDA 510(k) clearance?
HSA-SOLUTION, MODEL 10034/10064 received FDA 510(k) clearance on 2002-09-06, under 510(k) number K021896.
Who is the listed applicant for HSA-SOLUTION, MODEL 10034/10064?
The FDA 510(k) record lists Vitrolife Sweden AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HSA-SOLUTION, MODEL 10034/10064?
The FDA product code for HSA-SOLUTION, MODEL 10034/10064 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 Vitrolife Sweden AB 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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