KEVOR-CURETTE— 510(k) K882404

Substantially Equivalent

Euro-Med Intl.

FDA 510(k) clearance K882404 for KEVOR-CURETTE, Substantially Equivalent on 1988-07-08. Applicant: Euro-Med Intl.. Device class: 2.

Clearance details

Applicant: Euro-Med Intl.
Product code: Code PCF
Device class: Class 2
Regulation: 21 CFR 884.1050
Advisory panel: Obstetrics/Gynecology
Date received: 1988-06-10
Decision date: 1988-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alameda, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code PCF

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K060320 — FEMECC ENDOCERVICAL CURETTE2006-07-28
K882606 — EURO-MED ENDO-CURETTE1988-07-25
K860796 — DISPO-URETTE1986-04-08

More clearances from Euro-Med Intl.

K883884 — PROSTATIC CORE-CUT NEEDLE1988-12-05
K854890 — HOOK PROBE1986-05-02
K854891 — KNIFE1986-05-02
K854894 — SPOON1986-05-02
K854895 — BASKET FORCEP1986-05-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.