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FDA 510(k)

RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590

K-Number: K020255 · 2002-09-18

Decision Date2002-09-18
Product CodeODA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590 is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2002-09-18 under 510(k) number K020255. The device is classified under product code ODA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590?

RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590 is a medical device that received FDA 510(k) clearance on 2002-09-18. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K020255.

When did RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590 receive FDA 510(k) clearance?

RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590 received FDA 510(k) clearance on 2002-09-18, under 510(k) number K020255.

Who is the listed applicant for RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590?

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

What is the FDA product code for RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590?

The FDA product code for RIWO NET OPERATING OPERATING CONTROL SYSTEM, MODEL #5590 is ODA.

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 Richard Wolf Medical Instruments 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.

View all 142 devices →

Related Devices (Code: ODA)

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

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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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