I.V. STARR KIT— 510(k) K912161
Substantially EquivalentMedical Device Inspection Co., Inc.
FDA 510(k) clearance K912161 for I.V. STARR KIT, Substantially Equivalent on 1991-10-08. Applicant: Medical Device Inspection Co., Inc..
Clearance details
- Applicant
- Medical Device Inspection Co., Inc.
- Product code
- Code LKB
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
Adverse events under product code LKB
product code LKB- Other
- 2
- Total
- 2
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.