SPOMA INTERNATIONAL CORPORATION— 510(k) K943352

Name: FDA 510(k) clearance K943352
Creator: U.S. Food and Drug Administration
Published: 1994-08-05

Substantially Equivalent

Spoma Intl. Corp.

FDA 510(k) clearance K943352 for SPOMA INTERNATIONAL CORPORATION, Substantially Equivalent on 1994-08-05. Applicant: Spoma Intl. Corp.. Device class: 1.

Clearance details

Applicant: Spoma Intl. Corp.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1994-07-12
Decision date: 1994-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rowland Heights, CA, US

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