STAK-CHEX PLUS RETICS— 510(k) K992887

Name: FDA 510(k) clearance K992887
Creator: U.S. Food and Drug Administration
Published: 1999-11-22

Substantially Equivalent

Streck Laboratories, Inc.

FDA 510(k) clearance K992887 for STAK-CHEX PLUS RETICS, Substantially Equivalent on 1999-11-22. Applicant: Streck Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Streck Laboratories, Inc.
Product code: Code GLQ
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 1999-08-27
Decision date: 1999-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Omaha, NE, US

Download summary PDF View on FDA.gov ↗

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K090137 — STAK-CHEX PLUS RETICS2009-03-18
K000945 — PARA 12 PLUS RETICS2000-04-18

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K023656 — SICKLE-CHEX SOLUBILITY KIT2002-12-30
K021922 — MODIFICATION TO PARA 5X2002-06-25

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