Last synced on 14 November 2025 at 11:06 pm

REPROCESSED SEALED ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K012678
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2002
Days to Decision
365 days
Submission Type
Summary

REPROCESSED SEALED ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K012678
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2002
Days to Decision
365 days
Submission Type
Summary