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FDA 510(k)

CORNER SEAT

K-Number: K894767 · 1990-01-17

ApplicantCanadian Posture and Seating Centre, Inc.
Decision Date1990-01-17
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CORNER SEAT is the device name listed in this FDA 510(k) record. The listed applicant is Canadian Posture and Seating Centre, Inc.. It received FDA 510(k) clearance on 1990-01-17 under 510(k) number K894767. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNER SEAT?

CORNER SEAT is a medical device that received FDA 510(k) clearance on 1990-01-17. The listed applicant is Canadian Posture and Seating Centre, Inc.. The 510(k) number is K894767.

When did CORNER SEAT receive FDA 510(k) clearance?

CORNER SEAT received FDA 510(k) clearance on 1990-01-17, under 510(k) number K894767.

Who is the listed applicant for CORNER SEAT?

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 CORNER SEAT?

The FDA product code for CORNER SEAT is INN.

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.

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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.

K894770PERSONAL BACK WITH FIP KIT

Related Devices (Code: INN)

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.

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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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