Last synced on 14 November 2025 at 11:06 pm

REGULATOR FLOWMETER

Page Type
Cleared 510(K)
510(k) Number
K915505
510(k) Type
Traditional
Applicant
LIFEGUARD MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1992
Days to Decision
135 days
Submission Type
Statement

REGULATOR FLOWMETER

Page Type
Cleared 510(K)
510(k) Number
K915505
510(k) Type
Traditional
Applicant
LIFEGUARD MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1992
Days to Decision
135 days
Submission Type
Statement