KREDA DISC— 510(k) K874252

Substantially Equivalent

Richmond Products, Inc.

FDA 510(k) clearance K874252 for KREDA DISC, Substantially Equivalent on 1988-01-27. Applicant: Richmond Products, Inc.. Device class: 1.

Clearance details

Applicant: Richmond Products, Inc.
Product code: Code HOQ
Device class: Class 1
Regulation: 21 CFR 886.1330
Advisory panel: Ophthalmic
Date received: 1987-10-19
Decision date: 1988-01-27
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.

K874250 — THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.1988-01-11
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Data sourced from openFDA. This site is unofficial and independent of the FDA.