FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SHEATH, CYSTOURETHROSCOPE W/ OBTURATOR

K Number: K760179 · Decision Dec 2, 1976
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
91
Applicant Total
41
Review Days
149

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Basic Information

Device Name
SHEATH, CYSTOURETHROSCOPE W/ OBTURATOR
K Number
K760179
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Date Received
July 6, 1976
Decision Date
December 2, 1976
Product Code
FAJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FAJ Cystoscope And Accessories, Flexible/Rigid

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OES ELITE Cystoscope and Accessories; Obturator, 17 Fr. (WA2C17BO); Obturator, 19.8 Fr. (WA2C19BO); Obturator, 21 Fr. (WA2C21BO); Obturator, 21 Fr., for sheath with ramp (WA2C21RO); Obturator, 21 Fr., long (WA2C21LO); Obturator, 21 Fr., for straight sheath (WA2C21SO); Obturator, 22.5 Fr. (WA2C22BO); Obturator, 25 Fr. (WA2C25BO); Obturator, optical, 19.8 Fr. (WA2C19BV); Obturator, optical, 21 Fr. (WA2C21BV); Obturator, optical, 21 Fr., for straight sheath (WA2C21SV); Obturator, optical,

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Other Clearances by V. Mueller O.V. Baxter Healthcare Corp.

K Number Device Name
K803292 FIELD SUCTION DISSECTOR
K792383 KELMAN DIPSTICK
K771197 NORTON ENDOTRACHEAL
K771302 PFISTER-SCHWARTZ STONE RETRIEVER
K770959 BOUGIE, FILIFORM, JACKSON
K770280 CORD, ELECTROSURGICAL-STERILE & DISPOS.
K760851 CONVERSE ALTAR RETRACTOR
K761242 TEFLON COATED RESECTOSCOPE SHEATH
K760273 LITHOTRITE
K760172 OBTURATOR, VISUAL
Search all 41 clearances from V. Mueller O.V. Baxter Healthcare Corp. →