FAX — Bougie, Urological Class I

FDA Device Classification

FDA product code FAX covers "Bougie, Urological", a Class I medical device regulated under 21 CFR 876.5520. Submissions are reviewed by the Gastroenterology, Urology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
FAX
Device Class
Class I
Regulation Number
876.5520
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K950125karl storz endoscopy-americaKARL STORZ BOUGIES AND DILATORSFebruary 7, 1995
K822711parker laboratoriesANTI-MIST, ANTI-FOG EYEGLASS & DENTALNovember 3, 1982