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FDA 510(k)

V-LINK

K-Number: K903608 · 1990-10-12

ApplicantGE Medical Systems
Decision Date1990-10-12
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

V-LINK is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K903608. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-LINK?

V-LINK is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is GE Medical Systems. The 510(k) number is K903608.

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

V-LINK received FDA 510(k) clearance on 1990-10-12, under 510(k) number K903608.

Who is the listed applicant for V-LINK?

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

What is the FDA product code for V-LINK?

The FDA product code for V-LINK is CAW.

Other records listing GE Medical Systems as applicant

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Related Devices (Code: CAW)

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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