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

VALTRAC (BAR) REMOVER DEVICE

K Number: K863752 · Decision Oct 24, 1986
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
20
Applicant Total
45
Review Days
29

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Basic Information

Device Name
VALTRAC (BAR) REMOVER DEVICE
K Number
K863752
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Davis & Geck, Inc.
Date Received
September 25, 1986
Decision Date
October 24, 1986
Product Code
EMF
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
EMF Knife, Surgical

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Other Clearances by Davis & Geck, Inc.

K Number Device Name
K982853 SILK SUTURE
K981582 SURGILON, DERMALON, & OPHTHALON
K980610 DEXON RAPID (DEXON R)
K974015 ARGYLE QUICK- PICC PERIPHERALLY INSERTED CENTRAL CATHETER- PICC TRAYS, ARGYLE QUICK- PICC PERIPHERALLY INSERTED CENTRAL
K980062 MONOJECTT BLUNTIP I.V. ACCESS CANNULA WITH VIAL ACCESS PIN DEVICE
K973409 KANGAROO ENTERAL FEEDING EXTENSION SET FOR SYRINGE PUMPS
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)
Search all 45 clearances from Davis & Geck, Inc. →