POS-T-VAC ID-300— 510(k) K961309
Substantially EquivalentPos-T-Vac, Inc.
FDA 510(k) clearance K961309 for POS-T-VAC ID-300, Substantially Equivalent on 1996-06-10. Applicant: Pos-T-Vac, Inc..
Clearance details
- Applicant
- Pos-T-Vac, Inc.
- Product code
- Code KZH
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Adverse events under product code KZH
product code KZH- Other
- 1
- Total
- 1
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.