STERILIZATION PROCESS/BABY BLANKET— 510(k) K792626

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

1979-12-19

Decision date

1980-01-16

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Mchenry, IL, US

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