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

FIELD SUCTION DISSECTOR

K Number: K803292 · Decision Jan 29, 1981
Classifications
1
FEI Numbers
274
Registration Numbers
274
Same Product Code
6
Applicant Total
41
Review Days
30

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Basic Information

Device Name
FIELD SUCTION DISSECTOR
K Number
K803292
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Date Received
December 30, 1980
Decision Date
January 29, 1981
Product Code
GDI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GDI Dissector, Surgical, General & Plastic Surgery

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K760851 CONVERSE ALTAR RETRACTOR
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K760273 LITHOTRITE
K760172 OBTURATOR, VISUAL
K760180 FORCEPS, GRASPING
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