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

NEWMAN CANNULAE SYSTEM (NCS)

K Number: K862936 · Decision Aug 14, 1986
Classifications
1
FEI Numbers
378
Registration Numbers
378
Same Product Code
35
Applicant Total
27
Review Days
10

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Basic Information

Device Name
NEWMAN CANNULAE SYSTEM (NCS)
K Number
K862936
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent for Some Indications
Applicant
Byron Medical
Date Received
August 4, 1986
Decision Date
August 14, 1986
Product Code
GEA
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
GEA Cannula, Surgical, General & Plastic Surgery

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Other Clearances by Byron Medical

K Number Device Name
K040149 PSI-TEC PERISTALTIC INFILTRATION PUMP
K001803 ACCELERATOR RECIPROCATING CANNULA
K981215 PSI-TEC LIPOSUCTION ASPIRATOR
K981172 LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLES
K980738 PSI-TEC SYRINGE INFUSION PUMP AND ACCESSORIES FOR GENERAL FLUID IRRIGAION/INFILTRATION
K980392 PSI-TEC ASPIRATOR
K974295 BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING
K973133 BIG BAG 3000 PRESSURE INFUSOR
K934179 DISPOSABLE BAG DECANTER
K934233 ZARA ZONE IV MALAR IMPLANT MODIFICATION
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