Cleared Traditional

K891968 - ESP RADIATION REDUCTION EXAMINATION GLOVES (FDA 510(k) Clearance)

May 1989
Decision
54d
Days
Class 1
Risk

K891968 is an FDA 510(k) clearance for the ESP RADIATION REDUCTION EXAMINATION GLOVES. This device is classified as a Medical Glove, Specialty (Class I - General Controls, product code LZC).

Submitted by Boston Scientific Corp (Watertown, US). The FDA issued a Cleared decision on May 22, 1989, 54 days after receiving the submission on March 29, 1989.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.6250. A Disposable Medical Glove (examination Or Surgeon’s) Is A Device That May Or May Not Bear A Trace Amount Of Residual Powder And Is Intended To Be Worn On The Hand Or Finger(s) For Medical Purposes To Prevent Contamination. In Addition, These Gloves May Have Specialty Claims Such As Chemotherapy, Etc..

Submission Details

510(k) Number K891968 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 29, 1989
Decision Date May 22, 1989
Days to Decision 54 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary

Device Classification

Product Code LZC — Medical Glove, Specialty
Device Class Class I - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Disposable Medical Glove (examination Or Surgeon’s) Is A Device That May Or May Not Bear A Trace Amount Of Residual Powder And Is Intended To Be Worn On The Hand Or Finger(s) For Medical Purposes To Prevent Contamination. In Addition, These Gloves May Have Specialty Claims Such As Chemotherapy, Etc.