MANUAL RECLINING CHAIR
K-Number: K921028 · 1993-03-24
Advertisement
Device Summary
Frequently Asked Questions
What is the MANUAL RECLINING CHAIR?
MANUAL RECLINING CHAIR is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Labac Systems, Inc.. The 510(k) number is K921028.
When did MANUAL RECLINING CHAIR receive FDA 510(k) clearance?
MANUAL RECLINING CHAIR received FDA 510(k) clearance on 1993-03-24, under 510(k) number K921028.
Who is the listed applicant for MANUAL RECLINING CHAIR?
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 RECLINING CHAIR?
The FDA product code for MANUAL RECLINING CHAIR is IOR.
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: IOR)
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.
Advertisement