Last synced on 24 June 2022 at 11:05 pm

CAREPAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942350
510(k) Type
Traditional
Applicant
PRECISION MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1994
Days to Decision
203 days
Submission Type
Statement

CAREPAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942350
510(k) Type
Traditional
Applicant
PRECISION MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1994
Days to Decision
203 days
Submission Type
Statement