Last synced on 2 December 2022 at 11:04 pm

MODEL 2500 PNEUMATIC PERCUSSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802399
510(k) Type
Traditional
Applicant
MEDICAL EQUIPMENT DEVELOPMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1980
Days to Decision
21 days

MODEL 2500 PNEUMATIC PERCUSSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802399
510(k) Type
Traditional
Applicant
MEDICAL EQUIPMENT DEVELOPMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1980
Days to Decision
21 days