Last synced on 14 November 2025 at 11:06 pm

CREST PRESSURE INFUSOR

Page Type
Cleared 510(K)
510(k) Number
K822434
510(k) Type
Traditional
Applicant
CREST MEDICAL EQUIPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1982
Days to Decision
35 days

CREST PRESSURE INFUSOR

Page Type
Cleared 510(K)
510(k) Number
K822434
510(k) Type
Traditional
Applicant
CREST MEDICAL EQUIPMENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1982
Days to Decision
35 days