EHL PULSE GENERATOR— 510(k) K931779
Substantially EquivalentPsi Medical Products, Inc.
FDA 510(k) clearance K931779 for EHL PULSE GENERATOR, Substantially Equivalent on 1994-02-15. Applicant: Psi Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Psi Medical Products, Inc.
- Product code
- Code FFK
- Device class
- Class 2
- Regulation
- 21 CFR 876.4480
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, US
Recent devices under product code FFK
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