'E' CUBE AND 'E' PAD— 510(k) K873916

Substantially Equivalent

Richmond Products, Inc.

FDA 510(k) clearance K873916 for 'E' CUBE AND 'E' PAD, Substantially Equivalent on 1987-12-11. Applicant: Richmond Products, Inc.. Device class: 1.

Clearance details

Applicant: Richmond Products, Inc.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 1987-09-25
Decision date: 1987-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Richmond Products, Inc.

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K873907 — CONFIRMATION TESTS1987-12-29
K873908 — H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.1987-12-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.