GOLDLENS(TM)— 510(k) K913239

Substantially Equivalent

Doran Instruments, Inc.

FDA 510(k) clearance K913239 for GOLDLENS(TM), Substantially Equivalent on 1992-01-31. Applicant: Doran Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Doran Instruments, Inc.
Product code: Code HLZ
Device class: Class 2
Regulation: 21 CFR 886.1220
Advisory panel: Ophthalmic
Date received: 1991-07-22
Decision date: 1992-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Littleton, MA, US

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