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

TRU-CUT BIOPSY/ASPIRA-NEEDLE 2N2709

K Number: K831392 · Decision Jul 12, 1983
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
206
Review Days
74

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Basic Information

Device Name
TRU-CUT BIOPSY/ASPIRA-NEEDLE 2N2709
K Number
K831392
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Travenol Laboratories, S.A.
Date Received
April 29, 1983
Decision Date
July 12, 1983
Product Code
GAA
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
GAA Needle, Aspiration And Injection, Disposable

Similar 510(k) Clearances

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Other Clearances by Travenol Laboratories, S.A.

K Number Device Name
K874181 BAXTER BEDSIDE SYSTEM
K873894 CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITE
K873873 RESUBMITTED MICRON TRANSFUSION FILTER
K873984 AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)
K872364 HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309
K872652 UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM
K870801 FLO-GARD 6200 VOLUMETRIC INFUSION/PUMPING BLOOD
K871908 IV ADMINISTRATION SET
K871471 CAPILLARY FLOW DIALYZERS MODELS ST-12 & ST-15
K865029 CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER
Search all 206 clearances from Travenol Laboratories, S.A. →