PATIENT EXAMINATION GLOVES— 510(k) K904443

Substantially Equivalent

Pisak Enterprise Co., Ltd.

FDA 510(k) clearance K904443 for PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1990-10-17. Applicant: Pisak Enterprise Co., Ltd.. Device class: 1.

Clearance details

Applicant
Pisak Enterprise Co., Ltd.
Product code
Code LYY
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Buffalo Grove, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code LYY

view all

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