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FDA 510(k)

RICHMOND VISUAL FIELD SCREENER

K-Number: K873912 · 1987-11-02

ApplicantRichmond Products, Inc.
Decision Date1987-11-02
Product CodeHOO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RICHMOND VISUAL FIELD SCREENER is the device name listed in this FDA 510(k) record. The listed applicant is Richmond Products, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K873912. The device is classified under product code HOO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICHMOND VISUAL FIELD SCREENER?

RICHMOND VISUAL FIELD SCREENER is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Richmond Products, Inc.. The 510(k) number is K873912.

When did RICHMOND VISUAL FIELD SCREENER receive FDA 510(k) clearance?

RICHMOND VISUAL FIELD SCREENER received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873912.

Who is the listed applicant for RICHMOND VISUAL FIELD SCREENER?

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

What is the FDA product code for RICHMOND VISUAL FIELD SCREENER?

The FDA product code for RICHMOND VISUAL FIELD SCREENER is HOO.

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Other records listing Richmond Products, Inc. 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.

K874252KREDA DISCK874250THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.K874251WORTH 4 DOT TEST DISTANCE C/W MUSCLE LIGHTK873907CONFIRMATION TESTSK873908H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.K873914ANIMATED FIXATION TOYS (DISTANCE AND NEARPOINT)

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Related Devices (Code: HOO)

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.

K941723WELCH ALLYN GLAUCOMA DETECTORWelch Allyn, Inc.K930448MARCO PROJECTION PERIMETERMarco Ophthalmic, Inc.K864467HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREENKeeler Instruments, Inc.K860115DIGILAB CAMBRIDGE PERIMETERBio-RadK832800AUTOMATIC TANGENT SCREEN 50CooperVision, Inc.

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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