BINOCULAR MAGNIFIER 2X— 510(k) K830774

Substantially Equivalent

Almore Intl., Inc.

FDA 510(k) clearance K830774 for BINOCULAR MAGNIFIER 2X, Substantially Equivalent on 1983-04-06. Applicant: Almore Intl., Inc.. Device class: 1.

Clearance details

Applicant: Almore Intl., Inc.
Product code: Code HKC
Device class: Class 1
Regulation: 21 CFR 886.5540
Advisory panel: Ophthalmic
Date received: 1983-03-11
Decision date: 1983-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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