UROMAT 2000— 510(k) K903395
Substantially EquivalentPausch Corp.
FDA 510(k) clearance K903395 for UROMAT 2000, Substantially Equivalent on 1990-08-30. Applicant: Pausch Corp.. Device class: 2.
Clearance details
- Applicant
- Pausch Corp.
- Product code
- Code IXR
- Device class
- Class 2
- Regulation
- 21 CFR 892.1980
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Little Silver, NJ, US
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