SDI PREPAX COUNTAPETTE KIT— 510(k) K892658

Name: FDA 510(k) clearance K892658
Creator: U.S. Food and Drug Administration
Published: 1989-05-24

Substantially Equivalent

Scientific Distributors, Inc.

FDA 510(k) clearance K892658 for SDI PREPAX COUNTAPETTE KIT, Substantially Equivalent on 1989-05-24. Applicant: Scientific Distributors, Inc.. Device class: 1.

Clearance details

Applicant: Scientific Distributors, Inc.
Product code: Code JCG
Device class: Class 1
Regulation: 21 CFR 864.8200
Advisory panel: Hematology
Date received: 1989-04-13
Decision date: 1989-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwood, MA, US

Download summary PDF View on FDA.gov ↗

More clearances from Scientific Distributors, Inc.

view all

K851320 — SDI PREPAX DILUKIT M.1985-07-05
K840044 — SDI PREPAX DILUKIT 29-10001984-03-09
K840041 — SDI PREPAX DILUKIT HW1984-03-05
K840038 — PREPAX DILUKIT PLUS1984-02-10
K840042 — SDI PREPAX DILUKIT CA1984-02-10

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