J.M. PATIENT EXAMINATION GLOVES— 510(k) K891624

Substantially Equivalent

Jann Maw (U.S.A.), Inc.

FDA 510(k) clearance K891624 for J.M. PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1990-01-22. Applicant: Jann Maw (U.S.A.), Inc.. Device class: 1.

Clearance details

Applicant
Jann Maw (U.S.A.), 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
Richardson, TX, US
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