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PATIENT CABLE

Page Type
Cleared 510(K)
510(k) Number
K932704
510(k) Type
Traditional
Applicant
SENTRY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1993
Days to Decision
207 days
Submission Type
Statement

PATIENT CABLE

Page Type
Cleared 510(K)
510(k) Number
K932704
510(k) Type
Traditional
Applicant
SENTRY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1993
Days to Decision
207 days
Submission Type
Statement