URINOSCOPY FUNNEL— 510(k) K871671

Name: FDA 510(k) clearance K871671
Creator: U.S. Food and Drug Administration
Published: 1987-05-20

Substantially Equivalent

Portable Medical Laboratories, Inc.

FDA 510(k) clearance K871671 for URINOSCOPY FUNNEL, Substantially Equivalent on 1987-05-20. Applicant: Portable Medical Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Portable Medical Laboratories, Inc.
Product code: Code GHO
Device class: Class 1
Regulation: 21 CFR 864.6160
Advisory panel: Hematology
Date received: 1987-04-28
Decision date: 1987-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Solana Beach, CA, US

Download summary PDF View on FDA.gov ↗

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