FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BOUGIE, FILIFORM, JACKSON

K Number: K770959 · Decision Jun 14, 1977
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
0
Applicant Total
41
Review Days
18

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Basic Information

Device Name
BOUGIE, FILIFORM, JACKSON
K Number
K770959
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4175
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Date Received
May 27, 1977
Decision Date
June 14, 1977
Product Code
KBI
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
KBI Bougie, Eustachian

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
K770280 CORD, ELECTROSURGICAL-STERILE & DISPOS.
K760851 CONVERSE ALTAR RETRACTOR
K761242 TEFLON COATED RESECTOSCOPE SHEATH
K760273 LITHOTRITE
K760172 OBTURATOR, VISUAL
K760180 FORCEPS, GRASPING
Search all 41 clearances from V. Mueller O.V. Baxter Healthcare Corp. →