FDA 510(k)

P-LINK

K-Number: K922313 · 1992-07-10

Decision Date1992-07-10

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

P-LINK is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Imaging. It received FDA 510(k) clearance on 1992-07-10 under 510(k) number K922313. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P-LINK?

P-LINK is a medical device that received FDA 510(k) clearance on 1992-07-10. The listed applicant is Virtual Imaging. The 510(k) number is K922313.

When did P-LINK receive FDA 510(k) clearance?

P-LINK received FDA 510(k) clearance on 1992-07-10, under 510(k) number K922313.

Who is the listed applicant for P-LINK?

The FDA 510(k) record lists Virtual Imaging as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P-LINK?

The FDA product code for P-LINK is KPS.

Other records listing Virtual Imaging 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.

K063262AMX4-50 AND AMX4-31 MOBILE DIGITAL DIAGNOSTIC RADIOGRAPHIC SYSTEMS K891695VIEW 1000 K864854VIEW(TM) IMAGE PROCESSING AND VIEWING STATION

Related Devices (Code: KPS)

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.