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FASTUBE NERVE REGENERATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850785
510(k) Type
Traditional
Applicant
RESEARCH MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1985
Days to Decision
134 days

FASTUBE NERVE REGENERATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850785
510(k) Type
Traditional
Applicant
RESEARCH MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1985
Days to Decision
134 days