KVM ISOTONIC FLUSH SOLUTION— 510(k) K883989

Name: FDA 510(k) clearance K883989
Creator: U.S. Food and Drug Administration
Published: 1988-10-12

Substantially Equivalent

Kvm Technologies, Inc.

FDA 510(k) clearance K883989 for KVM ISOTONIC FLUSH SOLUTION, Substantially Equivalent on 1988-10-12. Applicant: Kvm Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Kvm Technologies, Inc.
Product code: Code GIF
Device class: Class 1
Regulation: 21 CFR 864.8200
Advisory panel: Hematology
Date received: 1988-09-20
Decision date: 1988-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GIF

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K883990 — KVM ISOTONIC DILUENT1988-10-12
K882490 — HYCEL QUICK-LYSING HEMOGLOBIN REAGENT1988-07-25
K882267 — SYSMEX QUICKLYSER-II (QLS-200A)1988-07-12
K881130 — CELL-DYN ISOTONIC DILUENT1988-03-31
K873347 — CELL-DYN DIFF. SCREEN ISOTONIC DILUENT1987-09-09

More clearances from Kvm Technologies, Inc.

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K925666 — THERAPACER 30001993-03-09
K883991 — KVM HEMOGLOBIN LYSING REAGENT1988-10-12
K883992 — KVM PREPACK HEMATOLOGY REAGENT SET1988-10-12

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