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RESPIRACULT-STREP DEEP BED CULTURE PAD

Page Type
Cleared 510(K)
510(k) Number
K821659
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1982
Days to Decision
62 days

RESPIRACULT-STREP DEEP BED CULTURE PAD

Page Type
Cleared 510(K)
510(k) Number
K821659
510(k) Type
Traditional
Applicant
ORION DIAGNOSTICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1982
Days to Decision
62 days