Last synced on 14 November 2025 at 11:06 pm

SPIROMETER, MONITORING W/ALARM

Page Type
Cleared 510(K)
510(k) Number
K780064
510(k) Type
Traditional
Applicant
OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1978
Days to Decision
19 days

SPIROMETER, MONITORING W/ALARM

Page Type
Cleared 510(K)
510(k) Number
K780064
510(k) Type
Traditional
Applicant
OHIO MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1978
Days to Decision
19 days