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FDA 510(k)

VISTACAM OMNI AND VIASTCAM OMNI (IC)

K-Number: K974204 · 1998-01-08

ApplicantAir Techniques, Inc.
Decision Date1998-01-08
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VISTACAM OMNI AND VIASTCAM OMNI (IC) is the device name listed in this FDA 510(k) record. The listed applicant is Air Techniques, Inc.. It received FDA 510(k) clearance on 1998-01-08 under 510(k) number K974204. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTACAM OMNI AND VIASTCAM OMNI (IC)?

VISTACAM OMNI AND VIASTCAM OMNI (IC) is a medical device that received FDA 510(k) clearance on 1998-01-08. The listed applicant is Air Techniques, Inc.. The 510(k) number is K974204.

When did VISTACAM OMNI AND VIASTCAM OMNI (IC) receive FDA 510(k) clearance?

VISTACAM OMNI AND VIASTCAM OMNI (IC) received FDA 510(k) clearance on 1998-01-08, under 510(k) number K974204.

Who is the listed applicant for VISTACAM OMNI AND VIASTCAM OMNI (IC)?

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

What is the FDA product code for VISTACAM OMNI AND VIASTCAM OMNI (IC)?

The FDA product code for VISTACAM OMNI AND VIASTCAM OMNI (IC) is EIA.

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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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