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PROTECTIV SAFETY BLOOD COLLECTION NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001690
510(k) Type
Traditional
Applicant
Johnson & Johnson Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2000
Days to Decision
59 days
Submission Type
Summary

PROTECTIV SAFETY BLOOD COLLECTION NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001690
510(k) Type
Traditional
Applicant
Johnson & Johnson Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2000
Days to Decision
59 days
Submission Type
Summary