DONORMATIC (BLOOD COLLECTION DEVICE)— 510(k) K760743

Name: FDA 510(k) clearance K760743
Creator: U.S. Food and Drug Administration
Published: 1976-12-06

Substantially Equivalent

Lifeline Instruments, Inc.

FDA 510(k) clearance K760743 for DONORMATIC (BLOOD COLLECTION DEVICE), Substantially Equivalent on 1976-12-06. Applicant: Lifeline Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Lifeline Instruments, Inc.
Product code: Code KSQ
Device class: Class 1
Regulation: 21 CFR 864.9195
Advisory panel: Hematology
Date received: 1976-09-30
Decision date: 1976-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K802608 — HEMATIC BLOOD MIXER1980-12-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.