Last synced on 25 April 2025 at 11:05 pm

MODEL 20C W/AN AR-10A/U & RL-20A/U FOR ARTHROSCOP.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880216
510(k) Type
Traditional
Applicant
DIRECTED ENERGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1988
Days to Decision
44 days

MODEL 20C W/AN AR-10A/U & RL-20A/U FOR ARTHROSCOP.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880216
510(k) Type
Traditional
Applicant
DIRECTED ENERGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1988
Days to Decision
44 days