PD-PAK— 510(k) K933619
Substantially EquivalentGeneral Medical Mfg. Co.
FDA 510(k) clearance K933619 for PD-PAK, Substantially Equivalent on 1994-02-22. Applicant: General Medical Mfg. Co.. Device class: 2.
Clearance details
- Applicant
- General Medical Mfg. Co.
- Product code
- Code MLW
- Device class
- Class 2
- Regulation
- 21 CFR 876.5630
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Richmond, VA, US
Recent devices under product code MLW
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