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

KEVOR-CURETTE

K Number: K882404 · Decision Jul 8, 1988
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
4
Applicant Total
16
Review Days
28

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Basic Information

Device Name
KEVOR-CURETTE
K Number
K882404
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1050
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Euro-Med Intl.
Date Received
June 10, 1988
Decision Date
July 8, 1988
Product Code
PCF
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
PCF Sampler, Endocervical

Similar 510(k) Clearances

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

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Other Clearances by Euro-Med Intl.

K Number Device Name
K883884 PROSTATIC CORE-CUT NEEDLE
K854894 SPOON
K854891 KNIFE
K854890 HOOK PROBE
K854898 ATLANTIC GRASPER
K854895 BASKET FORCEP
K854901 PACIFIC GRASPER
K854897 MAX-I-GRASP
K854896 HOOK SCISSOR
K854889 FLEX-I-GRASP
Search all 16 clearances from Euro-Med Intl. →