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MICK HDR INTERSTITIAL IMPLANT ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051423
510(k) Type
Traditional
Applicant
MICK RADIO-NUCLEAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2005
Days to Decision
30 days
Submission Type
Summary

MICK HDR INTERSTITIAL IMPLANT ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051423
510(k) Type
Traditional
Applicant
MICK RADIO-NUCLEAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2005
Days to Decision
30 days
Submission Type
Summary