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FDA 510(k)

CONTEXT FILTER

K-Number: K791108 · 1979-07-17

ApplicantGeometric Data, Div. Smithkline Corp.
Decision Date1979-07-17
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CONTEXT FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Geometric Data, Div. Smithkline Corp.. It received FDA 510(k) clearance on 1979-07-17 under 510(k) number K791108. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTEXT FILTER?

CONTEXT FILTER is a medical device that received FDA 510(k) clearance on 1979-07-17. The listed applicant is Geometric Data, Div. Smithkline Corp.. The 510(k) number is K791108.

When did CONTEXT FILTER receive FDA 510(k) clearance?

CONTEXT FILTER received FDA 510(k) clearance on 1979-07-17, under 510(k) number K791108.

Who is the listed applicant for CONTEXT FILTER?

The FDA 510(k) record lists Geometric Data, Div. Smithkline Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTEXT FILTER?

The FDA product code for CONTEXT FILTER is GKZ.

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Other records listing Geometric Data, Div. Smithkline Corp. 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.

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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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