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FDA 510(k)

MANUAL RECLINING CHAIR

K-Number: K921028 · 1993-03-24

Decision Date1993-03-24
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MANUAL RECLINING CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Labac Systems, Inc.. It received FDA 510(k) clearance on 1993-03-24 under 510(k) number K921028. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 11 devices →

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.

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