STERILIZATION PROCESS/X-RAY DETECT. SPG— 510(k) K792630

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K792630 for STERILIZATION PROCESS/X-RAY DETECT. SPG, Substantially Equivalent on 1980-01-11. Applicant: Procter & Gamble Mfg. Co..

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code GDY
Advisory panel: General, Plastic Surgery
Date received: 1979-12-19
Decision date: 1980-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code GDY

product code GDY

Malfunction: 764
Total: 764

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.