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SMARTSTITCH M-CONNECTOR, MODEL OM-8700; NEEDLE CASSETTE, OM-8750; AUTOCUFF SYSTEM INSTRUMENT SET, OM-9070

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033317
510(k) Type
Traditional
Applicant
Opus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2003
Days to Decision
76 days
Submission Type
Statement

SMARTSTITCH M-CONNECTOR, MODEL OM-8700; NEEDLE CASSETTE, OM-8750; AUTOCUFF SYSTEM INSTRUMENT SET, OM-9070

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033317
510(k) Type
Traditional
Applicant
Opus Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2003
Days to Decision
76 days
Submission Type
Statement