TILT SEATING SYSTEM
K-Number: K923366 · 1993-02-12
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Device Summary
Frequently Asked Questions
What is the TILT SEATING SYSTEM?
TILT SEATING SYSTEM is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Labac Systems, Inc.. The 510(k) number is K923366.
When did TILT SEATING SYSTEM receive FDA 510(k) clearance?
TILT SEATING SYSTEM received FDA 510(k) clearance on 1993-02-12, under 510(k) number K923366.
Who is the listed applicant for TILT SEATING SYSTEM?
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 TILT SEATING SYSTEM?
The FDA product code for TILT SEATING SYSTEM 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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