UROVIEW— 510(k) K872022
Substantially EquivalentOec-Diasonics, Inc.
FDA 510(k) clearance K872022 for UROVIEW, Substantially Equivalent on 1987-07-16. Applicant: Oec-Diasonics, Inc.. Device class: 1.
Clearance details
- Applicant
- Oec-Diasonics, Inc.
- Product code
- Code KQS
- Device class
- Class 1
- Regulation
- 21 CFR 876.4890
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
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