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SUSPENDER ORTHOPEDIC SUSPENSION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860037
510(k) Type
Traditional
Applicant
COMFORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1986
Days to Decision
15 days

SUSPENDER ORTHOPEDIC SUSPENSION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860037
510(k) Type
Traditional
Applicant
COMFORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1986
Days to Decision
15 days