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

DAVIS+GECK ABSORBABLE LIGATING DEVICE

K Number: K925602 · Decision Jul 8, 1993
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
45
Review Days
245

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Basic Information

Device Name
DAVIS+GECK ABSORBABLE LIGATING DEVICE
K Number
K925602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Davis & Geck, Inc.
Date Received
November 5, 1992
Decision Date
July 8, 1993
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

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K970857 ARGYLE AQUA-SEAL ALL PURPOSE AUTOTRANSFUSION CHEST DRAINAGE UNIT AND OPTIONAL ARGYLE AQUA-SEAL EVACUATING AUTOTRANSFUSIO
K972139 ASPR-CARE CLOSED SYSTEM,DUAL SWIVEL PIECE T,SHEATHED SUCTION CATHETER,BRONCHOSOPE ADAPTER,IN-LINE SPECIMEN TRAP
K972566 DEXON VIOLET
K962971 POLYPROPYLENE MESH (VARIOUS SIZES)
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