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SEIRIN JR ACUPUNCTURE NEEDLES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970260
510(k) Type
Traditional
Applicant
Seirin-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1997
Days to Decision
18 days
Submission Type
Summary

SEIRIN JR ACUPUNCTURE NEEDLES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970260
510(k) Type
Traditional
Applicant
Seirin-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1997
Days to Decision
18 days
Submission Type
Summary