Last synced on 18 April 2025 at 11:05 pm

FLEXIFLO INTRODUCER (DIRECT STICK) GASTROSTOMY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884275
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
12/22/1988
Days to Decision
71 days

FLEXIFLO INTRODUCER (DIRECT STICK) GASTROSTOMY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884275
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
12/22/1988
Days to Decision
71 days