QUICKIE P100 SERIES— 510(k) K963382
Substantially EquivalentQuickie Designs, Inc.
FDA 510(k) clearance K963382 for QUICKIE P100 SERIES, Substantially Equivalent on 1997-04-28. Applicant: Quickie Designs, Inc.. Device class: 2.
Clearance details
- Applicant
- Quickie Designs, Inc.
- Product code
- Code ITI
- Device class
- Class 2
- Regulation
- 21 CFR 890.3860
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fresno, CA, US
Recent devices under product code ITI
view allMore clearances from Quickie Designs, Inc.
view allAdverse events under product code ITI
product code ITI- Death
- 34
- Injury
- 778
- Malfunction
- 1,085
- Other
- 1
- Total
- 1,898
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.