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IOP8 INTRA OPERATIVE PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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