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QUINTREX 0515 PROGRAMMABLE PULSE GEN.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802223
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
9/12/1980
Days to Decision
0 days

QUINTREX 0515 PROGRAMMABLE PULSE GEN.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802223
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
9/12/1980
Days to Decision
0 days