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FDA 510(k)

H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.

K-Number: K873908 · 1987-12-23

ApplicantRichmond Products, Inc.
Decision Date1987-12-23
Product CodeHIT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK. 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 1987-12-23 under 510(k) number K873908. The device is classified under product code HIT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.?

H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK. is a medical device that received FDA 510(k) clearance on 1987-12-23. The listed applicant is Richmond Products, Inc.. The 510(k) number is K873908.

When did H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK. receive FDA 510(k) clearance?

H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK. received FDA 510(k) clearance on 1987-12-23, under 510(k) number K873908.

Who is the listed applicant for H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.?

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 H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.?

The FDA product code for H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK. is HIT.

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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 TESTSK873914ANIMATED FIXATION TOYS (DISTANCE AND NEARPOINT)K873916'E' CUBE AND 'E' PAD

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Related Devices (Code: HIT)

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.

K903001SLIMCATH (TM)Gynopharma, Inc.K875026ANOMALOSCOPE PLATE TEST - 5 [APT-5]Lkc Technologies, Inc.K873911PSEUDO ISOCHROMATIC COLOR BLINDNESS TEST BOOK - 15Richmond Products, Inc.K844694TITMUS VISION TESTER IITitmus Optical, Inc.K844365COLOR VISION TESTERSLuneau LaboratoriesK832843OSCAR COLOUR VISION TESTERKeeler Instruments, 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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