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INT — Plinth Class I

FDA Device Classification

Classification Details

Product Code
INT
Device Class
Class I
Regulation Number
890.3520
Submission Type
Review Panel
PM
Medical Specialty
Physical Medicine
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K770723chattanooga pharmacalTABLE, TREATMENT, THERAPY, PHYSICALJuly 11, 1977
K770636i e industriesTABLE, EXAM & MANUPULATIONApril 15, 1977
K770609will rossTABLE, MASSAGE & TREATMHNT, FIXED HEIGHTApril 8, 1977
K770509will rossTABLE, MASSAGE AND TREATMENTApril 5, 1977