HEMA(PRO)TEC(TION)— 510(k) K885324

Name: FDA 510(k) clearance K885324
Creator: U.S. Food and Drug Administration
Published: 1989-02-17

Substantially Equivalent

Medical Products Search, Inc.

FDA 510(k) clearance K885324 for HEMA(PRO)TEC(TION), Substantially Equivalent on 1989-02-17. Applicant: Medical Products Search, Inc.. Device class: 1.

Clearance details

Applicant: Medical Products Search, Inc.
Product code: Code GIO
Device class: Class 1
Regulation: 21 CFR 864.6150
Advisory panel: Hematology
Date received: 1988-12-28
Decision date: 1989-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Winston-Salem, NC, US

Download summary PDF View on FDA.gov ↗

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