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LKB 2160 MIDISPIN CENTRIFUGE

Page Type
Cleared 510(K)
510(k) Number
K831947
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1983
Days to Decision
43 days

LKB 2160 MIDISPIN CENTRIFUGE

Page Type
Cleared 510(K)
510(k) Number
K831947
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1983
Days to Decision
43 days