EYE SURGERY INSTRUMENT— 510(k) K840101

Name: FDA 510(k) clearance K840101
Creator: U.S. Food and Drug Administration
Published: 1984-03-16

Substantially Equivalent

Truline Instruments, Inc.

FDA 510(k) clearance K840101 for EYE SURGERY INSTRUMENT, Substantially Equivalent on 1984-03-16. Applicant: Truline Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Truline Instruments, Inc.
Product code: Code HOB
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1984-01-10
Decision date: 1984-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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