Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SINGLE CHAIR INTEGRAL BACK ATTACHMENT

K-Number: K922092 · 1992-05-26

Decision Date1992-05-26
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SINGLE CHAIR INTEGRAL BACK ATTACHMENT 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 1992-05-26 under 510(k) number K922092. 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 SINGLE CHAIR INTEGRAL BACK ATTACHMENT?

SINGLE CHAIR INTEGRAL BACK ATTACHMENT is a medical device that received FDA 510(k) clearance on 1992-05-26. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K922092.

When did SINGLE CHAIR INTEGRAL BACK ATTACHMENT receive FDA 510(k) clearance?

SINGLE CHAIR INTEGRAL BACK ATTACHMENT received FDA 510(k) clearance on 1992-05-26, under 510(k) number K922092.

Who is the listed applicant for SINGLE CHAIR INTEGRAL BACK ATTACHMENT?

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 SINGLE CHAIR INTEGRAL BACK ATTACHMENT?

The FDA product code for SINGLE CHAIR INTEGRAL BACK ATTACHMENT 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑