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FDA 510(k)

ROS-TR SYSTEM

K-Number: K873143 · 1987-09-11

ApplicantRoss Systems C/O Arent,Fox,Kintner,Plotkin,Kahn
Decision Date1987-09-11
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ROS-TR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn. It received FDA 510(k) clearance on 1987-09-11 under 510(k) number K873143. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROS-TR SYSTEM?

ROS-TR SYSTEM is a medical device that received FDA 510(k) clearance on 1987-09-11. The listed applicant is Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn. The 510(k) number is K873143.

When did ROS-TR SYSTEM receive FDA 510(k) clearance?

ROS-TR SYSTEM received FDA 510(k) clearance on 1987-09-11, under 510(k) number K873143.

Who is the listed applicant for ROS-TR SYSTEM?

The FDA 510(k) record lists Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROS-TR SYSTEM?

The FDA product code for ROS-TR SYSTEM is DZE.

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.

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Other records listing Ross Systems C/O Arent,Fox,Kintner,Plotkin,Kahn 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.

K884140ROS-TR SYSTEM

Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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