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INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K935561
510(k) Type
Traditional
Applicant
BAUSCH & LOMB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1994
Days to Decision
70 days
Submission Type
Statement

INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K935561
510(k) Type
Traditional
Applicant
BAUSCH & LOMB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1994
Days to Decision
70 days
Submission Type
Statement