Last synced on 6 June 2025 at 11:06 pm

MODEL 2100 ND:YAG SURGICAL LASER NEUROSURGICAL IND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861044
510(k) Type
Traditional
Applicant
SHARPLAN INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1986
Days to Decision
224 days

MODEL 2100 ND:YAG SURGICAL LASER NEUROSURGICAL IND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861044
510(k) Type
Traditional
Applicant
SHARPLAN INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1986
Days to Decision
224 days