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FDA 510(k)

ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM

K-Number: K923363 · 1993-03-24

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

Device Summary

ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM 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 K923363. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM?

ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM 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 K923363.

When did ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM receive FDA 510(k) clearance?

ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM received FDA 510(k) clearance on 1993-03-24, under 510(k) number K923363.

Who is the listed applicant for ADJUSTABLE SLIDING BACK POWER RECLINE 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 ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM?

The FDA product code for ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM is ITI.

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: ITI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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