Last synced on 14 November 2025 at 11:06 pm

CO2 RIGID LASER ENDOSCOPE PROBE SERIES 792/LAPARO

Page Type
Cleared 510(K)
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)
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