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FDA 510(k)

JACKSON CROSS CYLINDER TEST

K-Number: K873915 · 1987-10-28

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

Device Summary

JACKSON CROSS CYLINDER TEST 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 K873915. The device is classified under product code HOR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JACKSON CROSS CYLINDER TEST?

JACKSON CROSS CYLINDER TEST 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 K873915.

When did JACKSON CROSS CYLINDER TEST receive FDA 510(k) clearance?

JACKSON CROSS CYLINDER TEST received FDA 510(k) clearance on 1987-10-28, under 510(k) number K873915.

Who is the listed applicant for JACKSON CROSS CYLINDER TEST?

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 JACKSON CROSS CYLINDER TEST?

The FDA product code for JACKSON CROSS CYLINDER TEST is HOR.

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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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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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