FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300
K-Number: K983066 · 1998-11-27
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Device Summary
Frequently Asked Questions
What is the FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300?
FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300 is a medical device that received FDA 510(k) clearance on 1998-11-27. The listed applicant is Teftec Corp.. The 510(k) number is K983066.
When did FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300 receive FDA 510(k) clearance?
FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300 received FDA 510(k) clearance on 1998-11-27, under 510(k) number K983066.
Who is the listed applicant for FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300?
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 FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300?
The FDA product code for FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300 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 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.
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
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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