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FDA 510(k)

FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500

K-Number: K992627 · 1999-10-25

ApplicantTeftec Corp.
Decision Date1999-10-25
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500 is the device name listed in this FDA 510(k) record. The listed applicant is Teftec Corp.. It received FDA 510(k) clearance on 1999-10-25 under 510(k) number K992627. 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 FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500?

FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500 is a medical device that received FDA 510(k) clearance on 1999-10-25. The listed applicant is Teftec Corp.. The 510(k) number is K992627.

When did FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500 receive FDA 510(k) clearance?

FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500 received FDA 510(k) clearance on 1999-10-25, under 510(k) number K992627.

Who is the listed applicant for FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500?

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

What is the FDA product code for FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500?

The FDA product code for FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500 is ITI.

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Other records listing Teftec Corp. 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.

K022652ALPHATRAC, MODEL A 205K013307OMEGATRAC, MODEL Z105K993160OMEGA TRAC, MODEL Z100K992628FIRSTCLASS POWER TILT AND RECLINE SEAT SYSTEM, MODEL S400K983066FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300K982815ALPHATRAC, MODEL A200

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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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