MONOJECT SCALE MAGNIFIER— 510(k) K781459

Name: FDA 510(k) clearance K781459
Creator: U.S. Food and Drug Administration
Published: 1978-10-24

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K781459 for MONOJECT SCALE MAGNIFIER, Substantially Equivalent on 1978-10-24. Applicant: Sherwood Medical Industries. Device class: 1.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code HJY
Device class: Class 1
Regulation: 21 CFR 886.5800
Advisory panel: Ophthalmic
Date received: 1978-08-23
Decision date: 1978-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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