Last synced on 30 May 2025 at 11:05 pm

URETHAL CUTTER CLAMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820015
510(k) Type
Traditional
Applicant
LONE STAR MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1982
Days to Decision
48 days

URETHAL CUTTER CLAMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820015
510(k) Type
Traditional
Applicant
LONE STAR MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1982
Days to Decision
48 days