LENSOMETER MODEL 11— 510(k) K781440

Name: FDA 510(k) clearance K781440
Creator: U.S. Food and Drug Administration
Published: 1978-09-07

Substantially Equivalent

Rodenstock Instrument Corp.

FDA 510(k) clearance K781440 for LENSOMETER MODEL 11, Substantially Equivalent on 1978-09-07. Applicant: Rodenstock Instrument Corp.. Device class: 1.

Clearance details

Applicant: Rodenstock Instrument Corp.
Product code: Code HLM
Device class: Class 1
Regulation: 21 CFR 886.1425
Advisory panel: Ophthalmic
Date received: 1978-08-18
Decision date: 1978-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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