DONALDSON NATURAL EYEPATCH 'PATIENT PAK'— 510(k) K874411

Name: FDA 510(k) clearance K874411
Creator: U.S. Food and Drug Administration
Published: 1988-01-27

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K874411 for DONALDSON NATURAL EYEPATCH 'PATIENT PAK', Substantially Equivalent on 1988-01-27. Applicant: Keeler Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HMP
Device class: Class 1
Regulation: 21 CFR 878.4440
Advisory panel: General, Plastic Surgery
Date received: 1987-10-28
Decision date: 1988-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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