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FDA 510(k)

VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400

K-Number: K861698 · 1986-10-03

ApplicantVisiscan
Decision Date1986-10-03
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400 is the device name listed in this FDA 510(k) record. The listed applicant is Visiscan. It received FDA 510(k) clearance on 1986-10-03 under 510(k) number K861698. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400?

VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400 is a medical device that received FDA 510(k) clearance on 1986-10-03. The listed applicant is Visiscan. The 510(k) number is K861698.

When did VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400 receive FDA 510(k) clearance?

VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400 received FDA 510(k) clearance on 1986-10-03, under 510(k) number K861698.

Who is the listed applicant for VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400?

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

What is the FDA product code for VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400?

The FDA product code for VISISCAN CT SCANNERS - MODELS V600, V1200 & V2400 is JAK.

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Related Devices (Code: JAK)

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

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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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