REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS— 510(k) K033593
Substantially EquivalentClearmedical, Inc.
FDA 510(k) clearance K033593 for REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS, Substantially Equivalent on 2003-11-20. Applicant: Clearmedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Clearmedical, Inc.
- Product code
- Code NLU
- Device class
- Class 2
- Regulation
- 21 CFR 876.4300
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bellevue, WA, US
Recent devices under product code NLU
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