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FDA 510(k)

RIS SCANVIEW SYSTEM (RSVS)

K-Number: K970641 · 1997-05-02

Decision Date1997-05-02
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RIS SCANVIEW SYSTEM (RSVS) is the device name listed in this FDA 510(k) record. The listed applicant is Radiology Information Systems, Inc.. It received FDA 510(k) clearance on 1997-05-02 under 510(k) number K970641. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIS SCANVIEW SYSTEM (RSVS)?

RIS SCANVIEW SYSTEM (RSVS) is a medical device that received FDA 510(k) clearance on 1997-05-02. The listed applicant is Radiology Information Systems, Inc.. The 510(k) number is K970641.

When did RIS SCANVIEW SYSTEM (RSVS) receive FDA 510(k) clearance?

RIS SCANVIEW SYSTEM (RSVS) received FDA 510(k) clearance on 1997-05-02, under 510(k) number K970641.

Who is the listed applicant for RIS SCANVIEW SYSTEM (RSVS)?

The FDA 510(k) record lists Radiology Information Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIS SCANVIEW SYSTEM (RSVS)?

The FDA product code for RIS SCANVIEW SYSTEM (RSVS) is LMD.

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 Radiology Information Systems, Inc. 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: LMD)

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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