Cleared Traditional

K073257 - KAWASUMI LABORATORIES LARGE WING SETS WITH ANTINEEDLE STICK PROTECTOR (FDA 510(k) Clearance)

Jan 2008
Decision
67d
Days
Class 2
Risk

K073257 is an FDA 510(k) clearance for the KAWASUMI LABORATORIES LARGE WING SETS WITH ANTINEEDLE STICK PROTECTOR. This device is classified as a Needle, Hypodermic, Single Lumen (Class II - Special Controls, product code FMI).

Submitted by Kawasumi Laboratories, Inc. (Tampa, US). The FDA issued a Cleared decision on January 25, 2008, 67 days after receiving the submission on November 19, 2007.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.5570.

Submission Details

510(k) Number K073257 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 19, 2007
Decision Date January 25, 2008
Days to Decision 67 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FMI - Needle, Hypodermic, Single Lumen
Device Class Class II - Special Controls
CFR Regulation 21 CFR 880.5570