PERSONAL BACK WITH FIP KIT
K-Number: K894770 · 1989-09-11
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Device Summary
Frequently Asked Questions
What is the PERSONAL BACK WITH FIP KIT?
PERSONAL BACK WITH FIP KIT is a medical device that received FDA 510(k) clearance on 1989-09-11. The listed applicant is Canadian Posture and Seating Centre, Inc.. The 510(k) number is K894770.
When did PERSONAL BACK WITH FIP KIT receive FDA 510(k) clearance?
PERSONAL BACK WITH FIP KIT received FDA 510(k) clearance on 1989-09-11, under 510(k) number K894770.
Who is the listed applicant for PERSONAL BACK WITH FIP KIT?
The FDA 510(k) record lists Canadian Posture and Seating Centre, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERSONAL BACK WITH FIP KIT?
The FDA product code for PERSONAL BACK WITH FIP KIT 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 Canadian Posture and Seating Centre, 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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