HYDROBOOT— 510(k) K022233
Substantially EquivalentIncappe, Inc.
FDA 510(k) clearance K022233 for HYDROBOOT, Substantially Equivalent on 2002-08-12. Applicant: Incappe, Inc.. Device class: 2.
Clearance details
- Applicant
- Incappe, Inc.
- Product code
- Code DWL
- Device class
- Class 2
- Regulation
- 21 CFR 880.5780
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, NC, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.