Last synced on 20 May 2022 at 11:05 pm

MODIFIED ASSESS(R) PEAK FLOW METER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896953
510(k) Type
Traditional
Applicant
HEALTH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1990
Days to Decision
56 days

MODIFIED ASSESS(R) PEAK FLOW METER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896953
510(k) Type
Traditional
Applicant
HEALTH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1990
Days to Decision
56 days