LYSIS +— 510(k) K830186

Substantially Equivalent

Hematology Marketing Assoc.

FDA 510(k) clearance K830186 for LYSIS +, Substantially Equivalent on 1983-02-28. Applicant: Hematology Marketing Assoc.. Device class: 1.

Clearance details

Applicant: Hematology Marketing Assoc.
Product code: Code GGK
Device class: Class 1
Regulation: 21 CFR 864.8540
Advisory panel: Hematology
Date received: 1983-01-19
Decision date: 1983-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K863114 — PIASTRINIT1986-11-06

More clearances from Hematology Marketing Assoc.

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