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IOP8 INTRA OPERATIVE PROBE

Page Type
Cleared 510(K)
510(k) Number
K032315
510(k) Type
Traditional
Applicant
HUNTLEIGH HEALTHCARE, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/18/2004
Days to Decision
479 days
Submission Type
Summary

IOP8 INTRA OPERATIVE PROBE

Page Type
Cleared 510(K)
510(k) Number
K032315
510(k) Type
Traditional
Applicant
HUNTLEIGH HEALTHCARE, INC.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/18/2004
Days to Decision
479 days
Submission Type
Summary