Last synced on 25 November 2022 at 11:04 pm

BAUMAN CPR/RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904346
510(k) Type
Traditional
Applicant
GENERAL MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1990
Days to Decision
8 days

BAUMAN CPR/RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904346
510(k) Type
Traditional
Applicant
GENERAL MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1990
Days to Decision
8 days