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ANTINUCLEAR ANTOBODY CELL SUBSTRATE

Page Type
Cleared 510(K)
510(k) Number
K822607
510(k) Type
Traditional
Applicant
IMMULOK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1982
Days to Decision
21 days

ANTINUCLEAR ANTOBODY CELL SUBSTRATE

Page Type
Cleared 510(K)
510(k) Number
K822607
510(k) Type
Traditional
Applicant
IMMULOK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1982
Days to Decision
21 days