SINGLE-USE PATIENT UNDERPAD— 510(k) K862348
Substantially EquivalentProcter & Gamble Mfg. Co.
FDA 510(k) clearance K862348 for SINGLE-USE PATIENT UNDERPAD, Substantially Equivalent on 1986-07-02. Applicant: Procter & Gamble Mfg. Co..
Clearance details
- Applicant
- Procter & Gamble Mfg. Co.
- Product code
- Code KME
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.