MANUAL CHAIR BASE
K-Number: K921027 · 1992-03-20
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Device Summary
Frequently Asked Questions
What is the MANUAL CHAIR BASE?
MANUAL CHAIR BASE is a medical device that received FDA 510(k) clearance on 1992-03-20. The listed applicant is Labac Systems, Inc.. The 510(k) number is K921027.
When did MANUAL CHAIR BASE receive FDA 510(k) clearance?
MANUAL CHAIR BASE received FDA 510(k) clearance on 1992-03-20, under 510(k) number K921027.
Who is the listed applicant for MANUAL CHAIR BASE?
The FDA 510(k) record lists Labac Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MANUAL CHAIR BASE?
The FDA product code for MANUAL CHAIR BASE is KNN.
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 Labac Systems, 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: KNN)
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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