Last synced on 25 April 2025 at 11:05 pm

LIFESHIELD BLUNT CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963351
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1997
Days to Decision
184 days
Submission Type
Statement

LIFESHIELD BLUNT CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963351
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1997
Days to Decision
184 days
Submission Type
Statement