Last synced on 21 June 2024 at 11:04 pm

ENDOSCOPIC RETRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931092
510(k) Type
Traditional
Applicant
LASER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1993
Days to Decision
58 days
Submission Type
Statement