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

ELECTRODE, CUTTING LOOP

K Number: K760178 · Decision Oct 15, 1976
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
41
Review Days
101

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Basic Information

Device Name
ELECTRODE, CUTTING LOOP
K Number
K760178
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Date Received
July 6, 1976
Decision Date
October 15, 1976
Product Code
KNS
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
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

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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. →