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

STERILE SILICONE TUBING

K Number: K810071 · Decision Feb 12, 1981
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
26
Applicant Total
15
Review Days
30

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Basic Information

Device Name
STERILE SILICONE TUBING
K Number
K810071
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Medspec Corp.
Date Received
January 13, 1981
Decision Date
February 12, 1981
Product Code
GBS
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
GBS Catheter, Ventricular, General & Plastic Surgery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBS), ordered by most recent decision date.

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Other Clearances by Medspec Corp.

K Number Device Name
K813012 STERILE BASIN SETS
K812711 STERILE GAUZE PADS 12PLY
K812707 STERILE DISSECTOR SPONGES-X-RAY DETECT
K812710 STERILE LAPAROTOMY SPONGES-X-RAY DETECT
K812709 STERILE DENTAL ROLL
K810069 STERILE AIRWAY
K802060 STERILE TONSIL SPONGES
K801069 STERILE ISOLATION GOWN
K801068 STERILE ABDOMINAL PAD
K800278 MEDSPEC SAFETY PINS
Search all 15 clearances from Medspec Corp. →