LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED— 510(k) K982901

Substantially Equivalent

Vitalcare Group, Inc.

FDA 510(k) clearance K982901 for LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED, Substantially Equivalent on 1998-12-21. Applicant: Vitalcare Group, Inc.. Device class: 1.

Clearance details

Applicant
Vitalcare Group, Inc.
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
Miami, FL, US
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