BIODEX SYSTEM 2,MODEL S2-S
K-Number: K913020 · 1991-10-03
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Device Summary
Frequently Asked Questions
What is the BIODEX SYSTEM 2,MODEL S2-S?
BIODEX SYSTEM 2,MODEL S2-S is a medical device that received FDA 510(k) clearance on 1991-10-03. The listed applicant is Biodex Corp.. The 510(k) number is K913020.
When did BIODEX SYSTEM 2,MODEL S2-S receive FDA 510(k) clearance?
BIODEX SYSTEM 2,MODEL S2-S received FDA 510(k) clearance on 1991-10-03, under 510(k) number K913020.
Who is the listed applicant for BIODEX SYSTEM 2,MODEL S2-S?
The FDA 510(k) record lists Biodex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIODEX SYSTEM 2,MODEL S2-S?
The FDA product code for BIODEX SYSTEM 2,MODEL S2-S is IKK.
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 Biodex Corp. 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: IKK)
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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