DEXIDE DISPOSABLE SWAB STICK— 510(k) K791169

Name: FDA 510(k) clearance K791169
Creator: U.S. Food and Drug Administration
Published: 1979-07-30

Substantially Equivalent

Dexide, Inc.

FDA 510(k) clearance K791169 for DEXIDE DISPOSABLE SWAB STICK, Substantially Equivalent on 1979-07-30. Applicant: Dexide, Inc.. Device class: 1.

Clearance details

Applicant: Dexide, Inc.
Product code: Code KXF
Device class: Class 1
Regulation: 21 CFR 880.6025
Advisory panel: General Hospital
Date received: 1979-06-25
Decision date: 1979-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KXF

view all

K123184 — FINN CHAMBERS AQUA2012-12-19
K103409 — ALLERGEAZE R CLEAR2011-03-15
K063160 — ALLERGEAZE PATCH TEST CHAMBERS2006-12-22
K013820 — FINN CHAMBER (R)2002-01-30
K992553 — IQ CHAMBERS2000-04-12

More clearances from Dexide, Inc.

view all

K991814 — MULTACHOICE INSTRUMENTS1999-06-23
K990379 — MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES1999-03-04
K981940 — MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES1998-09-25
K981941 — MULTAPORT CANNULA REDUCER AND ACCESSORIES1998-07-29
K953611 — DEXIDE ENDO-LUBE KIT1995-09-15

Adverse events under product code KXF

product code KXF

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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