Last synced on 17 May 2024 at 11:06 pm

ATRAUMATIC STANDARD SPROTTE NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911260
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1991
Days to Decision
213 days

ATRAUMATIC STANDARD SPROTTE NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911260
510(k) Type
Traditional
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/1991
Days to Decision
213 days