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FDA 510(k)

BIODEX SYSTEM 2,MODEL S2-S

K-Number: K913020 · 1991-10-03

ApplicantBiodex Corp.
Decision Date1991-10-03
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BIODEX SYSTEM 2,MODEL S2-S is the device name listed in this FDA 510(k) record. The listed applicant is Biodex Corp.. It received FDA 510(k) clearance on 1991-10-03 under 510(k) number K913020. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 7 devices →

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

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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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