MAXCESS NEEDLEFREE - Y- SITE (100713)— 510(k) K970800
Substantially EquivalentSolopak Medical Products, Inc.
FDA 510(k) clearance K970800 for MAXCESS NEEDLEFREE - Y- SITE (100713), Substantially Equivalent on 1997-04-02. Applicant: Solopak Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Solopak Medical Products, Inc.
- Product code
- Code FPA
- Device class
- Class 2
- Regulation
- 21 CFR 880.5440
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Elk Grove Village, IL, US
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More clearances from Solopak Medical Products, Inc.
view allAdverse events under product code FPA
product code FPA- Death
- 95
- Injury
- 14,421
- Malfunction
- 125,815
- Other
- 30
- Total
- 140,361
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.