STERILIZATION PROCESS/ MAYO PAD— 510(k) K792624

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K792624 for STERILIZATION PROCESS/ MAYO PAD, Substantially Equivalent on 1980-01-11. Applicant: Procter & Gamble Mfg. Co.. Device class: 2.

Clearance details

Applicant
Procter & Gamble Mfg. Co.
Product code
Code JOJ
Device class
Class 2
Regulation
21 CFR 880.2800
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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