Last synced on 23 September 2022 at 11:05 pm

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881010
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1988
Days to Decision
42 days

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881010
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1988
Days to Decision
42 days