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

NORTON ENDOTRACHEAL

K Number: K771197 · Decision Aug 16, 1977
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
41
Review Days
46

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Basic Information

Device Name
NORTON ENDOTRACHEAL
K Number
K771197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Date Received
July 1, 1977
Decision Date
August 16, 1977
Product Code
BTR
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BTR Tube, Tracheal (W/Wo Connector)

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K Number Device Name
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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
K760180 FORCEPS, GRASPING
Search all 41 clearances from V. Mueller O.V. Baxter Healthcare Corp. →