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ALLOY SCALPEL HANDPIECES

Page Type
Cleared 510(K)
510(k) Number
K914197
510(k) Type
Traditional
Applicant
LASER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1992
Days to Decision
204 days
Submission Type
Statement

ALLOY SCALPEL HANDPIECES

Page Type
Cleared 510(K)
510(k) Number
K914197
510(k) Type
Traditional
Applicant
LASER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1992
Days to Decision
204 days
Submission Type
Statement