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

VISISTAT SKIN STAPLING DEVICE

K Number: K844837 · Decision Jan 23, 1985
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
18
Applicant Total
140
Review Days
42

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Basic Information

Device Name
VISISTAT SKIN STAPLING DEVICE
K Number
K844837
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4760
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Edward Weck, Inc.
Date Received
December 12, 1984
Decision Date
January 23, 1985
Product Code
GDT
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
GDT Staple, Removable (Skin)

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K902108 HEM-O-LOK(TM)
K902232 WECK ELECTROSURGICAL GENERATOR #174200
K897045 BOWIE-DICK TEST CARD CATALOG NUMBER 008018
K871110 CORONARY ARTERY BYPASS GRAFT (CABG) MARKER
K851251 AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200
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