PATIENT EXAMINATION GLOVES— 510(k) K890858

Substantially Equivalent

Rejuvena Ent. Co. , Ltd.

FDA 510(k) clearance K890858 for PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1989-07-14. Applicant: Rejuvena Ent. Co. , Ltd.. Device class: 1.

Clearance details

Applicant
Rejuvena Ent. 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
Taiwan R.O.C., TW
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