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WOM LAPAROFLATOR ELECTRONIC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921086
510(k) Type
Traditional
Applicant
W.O.M. GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/7/1992
Days to Decision
32 days
Submission Type
Statement