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FDA 510(k)

SAMSUNG RAYPAX DISPLAY WORKSTATION

K-Number: K992306 · 1999-09-22

ApplicantSamsung Sds Co., Ltd.
Decision Date1999-09-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SAMSUNG RAYPAX DISPLAY WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Samsung Sds Co., Ltd.. It received FDA 510(k) clearance on 1999-09-22 under 510(k) number K992306. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAMSUNG RAYPAX DISPLAY WORKSTATION?

SAMSUNG RAYPAX DISPLAY WORKSTATION is a medical device that received FDA 510(k) clearance on 1999-09-22. The listed applicant is Samsung Sds Co., Ltd.. The 510(k) number is K992306.

When did SAMSUNG RAYPAX DISPLAY WORKSTATION receive FDA 510(k) clearance?

SAMSUNG RAYPAX DISPLAY WORKSTATION received FDA 510(k) clearance on 1999-09-22, under 510(k) number K992306.

Who is the listed applicant for SAMSUNG RAYPAX DISPLAY WORKSTATION?

The FDA 510(k) record lists Samsung Sds Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAMSUNG RAYPAX DISPLAY WORKSTATION?

The FDA product code for SAMSUNG RAYPAX DISPLAY WORKSTATION is LLZ.

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Other records listing Samsung Sds Co., Ltd. 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.

K002062SAMSUNG 10DR IMPLANT SYSTEMK992426RAYPAX WEB CLINICAL SYSTEMK992131SAMSUNG RAYPAX LONG TERM ARCHIVEK992112SAMSUNG RAYPAX FILM DIGITIZERK991537SAMSUNG RAYPAX SYSTEM

Related Devices (Code: LLZ)

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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