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NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100520
510(k) Type
Special
Applicant
NIPRO MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2010
Days to Decision
22 days
Submission Type
Summary

NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100520
510(k) Type
Special
Applicant
NIPRO MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2010
Days to Decision
22 days
Submission Type
Summary