DIGIT WIDGET— 510(k) K992970
Substantially EquivalentHand Biomechanics Lab, Inc.
FDA 510(k) clearance K992970 for DIGIT WIDGET, Substantially Equivalent on 1999-11-08. Applicant: Hand Biomechanics Lab, Inc.. Device class: 2.
Clearance details
- Applicant
- Hand Biomechanics Lab, Inc.
- Product code
- Code JDW
- Device class
- Class 2
- Regulation
- 21 CFR 888.3040
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sacramento, CA, US
Recent devices under product code JDW
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Adverse events under product code JDW
product code JDW- Injury
- 717
- Total
- 717
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.