JOHNSON & JOHNSON TUBE SECUREMENT DEVICE— 510(k) K895431
Substantially EquivalentJohnson & Johnson Patient Care, Inc.
FDA 510(k) clearance K895431 for JOHNSON & JOHNSON TUBE SECUREMENT DEVICE, Substantially Equivalent on 1989-10-13. Applicant: Johnson & Johnson Patient Care, Inc..
Clearance details
- Applicant
- Johnson & Johnson Patient Care, Inc.
- Product code
- Code KMK
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Brunswick, NJ, US
Adverse events under product code KMK
product code KMK- Malfunction
- 461
- Other
- 1
- Total
- 462
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.