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ROMFLEX REHAB EQUIP CERVICAL FLEXOR UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910151
510(k) Type
Traditional
Applicant
DYNA FLEX, INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1991
Days to Decision
4 days

ROMFLEX REHAB EQUIP CERVICAL FLEXOR UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910151
510(k) Type
Traditional
Applicant
DYNA FLEX, INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1991
Days to Decision
4 days