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FDA 510(k)

HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER

K-Number: K891610 · 1989-06-05

ApplicantKeeler Instruments, Inc.
Decision Date1989-06-05
Product CodeHOD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1989-06-05 under 510(k) number K891610. The device is classified under product code HOD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER?

HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER is a medical device that received FDA 510(k) clearance on 1989-06-05. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K891610.

When did HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER receive FDA 510(k) clearance?

HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER received FDA 510(k) clearance on 1989-06-05, under 510(k) number K891610.

Who is the listed applicant for HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER?

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

What is the FDA product code for HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER?

The FDA product code for HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER is HOD.

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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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