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FDA 510(k)

TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR

K-Number: K922772 · 1992-07-13

Decision Date1992-07-13
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Biodan Medical Systems, Ltd.. It received FDA 510(k) clearance on 1992-07-13 under 510(k) number K922772. 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 TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR?

TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR is a medical device that received FDA 510(k) clearance on 1992-07-13. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K922772.

When did TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR receive FDA 510(k) clearance?

TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR received FDA 510(k) clearance on 1992-07-13, under 510(k) number K922772.

Who is the listed applicant for TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR?

The FDA 510(k) record lists Biodan Medical Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR?

The FDA product code for TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR 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 Biodan Medical Systems, Ltd. 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 20 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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