Last synced on 14 November 2025 at 11:06 pm

MODIFIED ASSESS(R) PEAK FLOW METER

Page Type
Cleared 510(K)
510(k) Number
K902292
510(k) Type
Traditional
Applicant
HEALTH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1990
Days to Decision
80 days

MODIFIED ASSESS(R) PEAK FLOW METER

Page Type
Cleared 510(K)
510(k) Number
K902292
510(k) Type
Traditional
Applicant
HEALTH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1990
Days to Decision
80 days