OPACITY LENSMETER 701— 510(k) K874355

Substantially Equivalent

Intraoptics, Inc.

FDA 510(k) clearance K874355 for OPACITY LENSMETER 701, Substantially Equivalent on 1988-01-26. Applicant: Intraoptics, Inc.. Device class: 2.

Clearance details

Applicant: Intraoptics, Inc.
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 1987-10-23
Decision date: 1988-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Huntington, WV, US

Download summary PDF View on FDA.gov ↗

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