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FDA 510(k)

TANGENT SCREEN

K-Number: K873919 · 1987-10-28

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

Device Summary

TANGENT SCREEN 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 K873919. The device is classified under product code HOJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TANGENT SCREEN?

TANGENT SCREEN 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 K873919.

When did TANGENT SCREEN receive FDA 510(k) clearance?

TANGENT SCREEN received FDA 510(k) clearance on 1987-10-28, under 510(k) number K873919.

Who is the listed applicant for TANGENT SCREEN?

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 TANGENT SCREEN?

The FDA product code for TANGENT SCREEN is HOJ.

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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: HOJ)

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.

K844657SPECTABLE FRAME MAGNIFYING BRILLETTEPro Design Intl. ASK821081CHART PROJECTORMedical Equipment Designs, 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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