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LATERAL FLEXION MACHINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940455
510(k) Type
Traditional
Applicant
REHAB, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/12/1995
Days to Decision
345 days
Submission Type
Statement

LATERAL FLEXION MACHINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940455
510(k) Type
Traditional
Applicant
REHAB, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/12/1995
Days to Decision
345 days
Submission Type
Statement