FENZL RETICLE— 510(k) K801733

Substantially Equivalent

Robert E. Fenzl, M.D.

FDA 510(k) clearance K801733 for FENZL RETICLE, Substantially Equivalent on 1980-09-16. Applicant: Robert E. Fenzl, M.D.. Device class: 1.

Clearance details

Applicant: Robert E. Fenzl, M.D.
Product code: Code HOI
Device class: Class 1
Regulation: 21 CFR 886.5840
Advisory panel: Ophthalmic
Date received: 1980-07-25
Decision date: 1980-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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