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FDA 510(k)

DIFFUSER PANEL

K-Number: K970240 · 1997-03-11

ApplicantFocused Viewer, Inc.
Decision Date1997-03-11
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIFFUSER PANEL is the device name listed in this FDA 510(k) record. The listed applicant is Focused Viewer, Inc.. It received FDA 510(k) clearance on 1997-03-11 under 510(k) number K970240. The device is classified under product code IXC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIFFUSER PANEL?

DIFFUSER PANEL is a medical device that received FDA 510(k) clearance on 1997-03-11. The listed applicant is Focused Viewer, Inc.. The 510(k) number is K970240.

When did DIFFUSER PANEL receive FDA 510(k) clearance?

DIFFUSER PANEL received FDA 510(k) clearance on 1997-03-11, under 510(k) number K970240.

Who is the listed applicant for DIFFUSER PANEL?

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

What is the FDA product code for DIFFUSER PANEL?

The FDA product code for DIFFUSER PANEL is IXC.

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Related Devices (Code: IXC)

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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