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FDA 510(k)

A-DEC KNEEBREAK 1030 CHAIR

K-Number: K913059 · 1991-10-08

ApplicantA-Dec, Inc.
Decision Date1991-10-08
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

A-DEC KNEEBREAK 1030 CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is A-Dec, Inc.. It received FDA 510(k) clearance on 1991-10-08 under 510(k) number K913059. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-DEC KNEEBREAK 1030 CHAIR?

A-DEC KNEEBREAK 1030 CHAIR is a medical device that received FDA 510(k) clearance on 1991-10-08. The listed applicant is A-Dec, Inc.. The 510(k) number is K913059.

When did A-DEC KNEEBREAK 1030 CHAIR receive FDA 510(k) clearance?

A-DEC KNEEBREAK 1030 CHAIR received FDA 510(k) clearance on 1991-10-08, under 510(k) number K913059.

Who is the listed applicant for A-DEC KNEEBREAK 1030 CHAIR?

The FDA 510(k) record lists A-Dec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-DEC KNEEBREAK 1030 CHAIR?

The FDA product code for A-DEC KNEEBREAK 1030 CHAIR is KLC.

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 A-Dec, Inc. 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 68 devices →

Related Devices (Code: KLC)

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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