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EXCELCARE PATIENT EXAMINATION GLOVES

K891500 Class I Traditional
Decision Date
1989-07-14
Sponsor / Applicant
Modern Health Care Products

Technical Specification

510(k) Submission ID K891500
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1989-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXCELCARE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance under submission number K891500, sponsored by Modern Health Care Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1989-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.