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SensiCare PI Ortho LT Surgical Glove (Tested for Use with Chemotherapy Drugs)

K203538 Class I Traditional
Decision Date
2021-08-02
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K203538
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2021-08-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SensiCare PI Ortho LT Surgical Glove (Tested for Use with Chemotherapy Drugs) received FDA 510(k) clearance under submission number K203538, sponsored by Medline Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2021-08-02.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.