BLADEWORKS DISPOSABLE ALK TUBING— 510(k) K993591

Name: FDA 510(k) clearance K993591
Creator: U.S. Food and Drug Administration
Published: 1999-12-28

Substantially Equivalent

Blade Works, Inc.

FDA 510(k) clearance K993591 for BLADEWORKS DISPOSABLE ALK TUBING, Substantially Equivalent on 1999-12-28. Applicant: Blade Works, Inc.. Device class: 1.

Clearance details

Applicant: Blade Works, Inc.
Product code: Code KYG
Device class: Class 1
Regulation: 21 CFR 886.4360
Advisory panel: Ophthalmic
Date received: 1999-10-22
Decision date: 1999-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Niguel, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYG

view all

K010353 — MED-LOGICS DISPOSABLE ALK TUBING2001-04-27
K003036 — TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,1010252000-12-22
K981116 — SOVEREIGN CATARACT EXTRACTION SYSTEM1998-05-19
K980647 — EYE IRRIGATOR MODEL #20201998-05-15
K974561 — MOISTAIR FLUID AIR TUBING SET1998-02-19

More clearances from Blade Works, Inc.

view all

K020079 — BLADEWORKS MICROKERATOME BLADE, MODEL 70612002-04-19
K993225 — BLADEWORKS MICROKERATOME BLADE2000-03-20

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