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KEELER MULTILASE 3000

Page Type
Cleared 510(K)
510(k) Number
K942180
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1994
Days to Decision
202 days
Submission Type
Statement

KEELER MULTILASE 3000

Page Type
Cleared 510(K)
510(k) Number
K942180
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1994
Days to Decision
202 days
Submission Type
Statement