FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FEMORAL CANAL SUCTION TAMPON

K Number: K831999 · Decision Sep 29, 1983
Classifications
1
FEI Numbers
331
Registration Numbers
331
Same Product Code
83
Applicant Total
4
Review Days
100

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Basic Information

Device Name
FEMORAL CANAL SUCTION TAMPON
K Number
K831999
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Richards Manufacturer Co.
Date Received
June 21, 1983
Decision Date
September 29, 1983
Product Code
JOL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOL Catheter And Tip, Suction

Similar 510(k) Clearances

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

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Other Clearances by Richards Manufacturer Co.

K Number Device Name
K831884 SPECTRON EXTRA-SMALL, STRAIGHT FEMORAL
K832000 THIGH HOLDER
K831656 ARTHROSCOPY KNIVES/PROBES/BENDING TOOL