A-DEC KNEEBREAK 1030 CHAIR
K-Number: K913059 · 1991-10-08
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Device Summary
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.
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
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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