Last synced on 16 May 2025 at 11:05 pm

LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792609
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1980
Days to Decision
337 days

LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792609
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1980
Days to Decision
337 days