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FDA 510(k)

READING CHARTS-CARDS (DISTANCE AND NEARPOINT)

K-Number: K873909 · 1987-10-28

ApplicantRichmond Products, Inc.
Decision Date1987-10-28
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

READING CHARTS-CARDS (DISTANCE AND NEARPOINT) 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 1987-10-28 under 510(k) number K873909. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the READING CHARTS-CARDS (DISTANCE AND NEARPOINT)?

READING CHARTS-CARDS (DISTANCE AND NEARPOINT) is a medical device that received FDA 510(k) clearance on 1987-10-28. The listed applicant is Richmond Products, Inc.. The 510(k) number is K873909.

When did READING CHARTS-CARDS (DISTANCE AND NEARPOINT) receive FDA 510(k) clearance?

READING CHARTS-CARDS (DISTANCE AND NEARPOINT) received FDA 510(k) clearance on 1987-10-28, under 510(k) number K873909.

Who is the listed applicant for READING CHARTS-CARDS (DISTANCE AND NEARPOINT)?

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 READING CHARTS-CARDS (DISTANCE AND NEARPOINT)?

The FDA product code for READING CHARTS-CARDS (DISTANCE AND NEARPOINT) is HOX.

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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: HOX)

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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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