HOOK PROBE— 510(k) K854890

Substantially Equivalent

Euro-Med Intl.

FDA 510(k) clearance K854890 for HOOK PROBE, Substantially Equivalent on 1986-05-02. Applicant: Euro-Med Intl.. Device class: 1.

Clearance details

Applicant: Euro-Med Intl.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-12-06
Decision date: 1986-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danville, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KDC

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K936226 — SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET1994-03-07
K920153 — THERMUFF BAG1992-07-01
K920263 — MANUAL SURGICAL INSTRUMENTS1992-05-06
K915064 — DISPOSABLE CAUTERY ABRASIVE PAD1992-03-11

More clearances from Euro-Med Intl.

K883884 — PROSTATIC CORE-CUT NEEDLE1988-12-05
K882404 — KEVOR-CURETTE1988-07-08
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.