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

NEZHAT-DORSEY REUSABLE ELECTROSURGICAL ATTACHMENTS: J-HOOK TIP, L-HOOK TIP, CORBITT SPATULA TIP, NEEDLE TIP, BALL TIP

K Number: K003674 · Decision Dec 8, 2000
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
24
Review Days
9

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Basic Information

Device Name
NEZHAT-DORSEY REUSABLE ELECTROSURGICAL ATTACHMENTS: J-HOOK TIP, L-HOOK TIP, CORBITT SPATULA TIP, NEEDLE TIP, BALL TIP
K Number
K003674
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Davol Inc., Sub. C. R. Bard, Inc.
Date Received
November 29, 2000
Decision Date
December 8, 2000
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
Y

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K081010 BARD 3DMAX MESH
K061754 BARD COMPOSITE L/P MESH
K061314 BARD EXTRA LARGE COMPOSIX KUGEL HERNIA PATCH
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K050610 SALUTE FIXATION SYSTEM
K011069 AQUASENS FLUID MONITORING SYSTEM
K991799 DAVOL HYSTEROSCOPY POUCH DRAPE AND TUBING SET, MODEL OOXXXXO
K991637 BARD SPERMA-TEX PRESHAPED MESH (2.4X5.6), MODEL 0114700
Search all 24 clearances from Davol Inc., Sub. C. R. Bard, Inc. →