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FDA 510(k)

BASIC TILT CHAIR ( BTC )

K-Number: K934418 · 1994-01-07

Decision Date1994-01-07
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BASIC TILT CHAIR ( BTC ) 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 1994-01-07 under 510(k) number K934418. 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 BASIC TILT CHAIR ( BTC )?

BASIC TILT CHAIR ( BTC ) is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Labac Systems, Inc.. The 510(k) number is K934418.

When did BASIC TILT CHAIR ( BTC ) receive FDA 510(k) clearance?

BASIC TILT CHAIR ( BTC ) received FDA 510(k) clearance on 1994-01-07, under 510(k) number K934418.

Who is the listed applicant for BASIC TILT CHAIR ( BTC )?

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 BASIC TILT CHAIR ( BTC )?

The FDA product code for BASIC TILT CHAIR ( BTC ) 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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