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FDA 510(k)

TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM

K-Number: K923365 · 1993-03-24

ApplicantLabsystems, Inc.
Decision Date1993-03-24
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Labsystems, Inc.. It received FDA 510(k) clearance on 1993-03-24 under 510(k) number K923365. 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 TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM?

TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Labsystems, Inc.. The 510(k) number is K923365.

When did TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM receive FDA 510(k) clearance?

TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM received FDA 510(k) clearance on 1993-03-24, under 510(k) number K923365.

Who is the listed applicant for TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM?

The FDA 510(k) record lists Labsystems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM?

The FDA product code for TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM is ITI.

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Other records listing Labsystems, Inc. as applicant

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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.

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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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