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LASER CENTERING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872747
510(k) Type
Traditional
Applicant
INNOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1987
Days to Decision
53 days

LASER CENTERING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872747
510(k) Type
Traditional
Applicant
INNOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1987
Days to Decision
53 days