ATTENDS DISPOS. UNDERPAD— 510(k) K853880

Clearance details

Applicant

Procter & Gamble Mfg. Co.

Product code

Code KME

Device class

Class 1

Regulation

21 CFR 880.6060

Advisory panel

General Hospital

Date received

1985-09-18

Decision date

1985-10-16

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Cincinnati, OH, US

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