Last synced on 14 November 2025 at 11:06 pm

LKB 2161 MIDISPIN R CENTRIFUGE

Page Type
Cleared 510(K)
510(k) Number
K831948
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 2161 MIDISPIN R CENTRIFUGE

Page Type
Cleared 510(K)
510(k) Number
K831948
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