Last synced on 23 May 2025 at 11:06 pm

LEADWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933603
510(k) Type
Traditional
Applicant
SENTRY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
175 days
Submission Type
Statement

LEADWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933603
510(k) Type
Traditional
Applicant
SENTRY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1994
Days to Decision
175 days
Submission Type
Statement