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LABELING FOR MYO/WIRE II STERNOTOMY SUTURES — Alto Development Corp. (510(k) K932513)

LABELING FOR MYO/WIRE II STERNOTOMY SUTURES — Alto Development Corp. (510(k) K932513) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: LABELING FOR MYO/WIRE II STERNOTOMY SUTURES; Applicant: Alto Development Corp.; Clearance track: 510(k).

Device nameLABELING FOR MYO/WIRE II STERNOTOMY SUTURES
ApplicantAlto Development Corp.
Clearance track510(k)
Submission numberK932513
DecisionSubstantially Equivalent
Decision date1994-01-07
Date received1993-05-25
Product codeGAO
Device class2
Medical specialtyGeneral, Plastic Surgery
Applicant locationNJ, US
SourceopenFDA device

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