Last synced on 20 December 2024 at 11:05 pm

NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924102
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1992
Days to Decision
104 days
Submission Type
Statement

NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924102
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1992
Days to Decision
104 days
Submission Type
Statement