STERILIZATION PROCESS CHANGE BOUNDARY— 510(k) K792621
Substantially EquivalentProcter & Gamble Mfg. Co.
FDA 510(k) clearance K792621 for STERILIZATION PROCESS CHANGE BOUNDARY, Substantially Equivalent on 1980-01-11. Applicant: Procter & Gamble Mfg. Co..
Clearance details
- Applicant
- Procter & Gamble Mfg. Co.
- Product code
- Code KKX
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.