KNIFE— 510(k) K854891

Substantially Equivalent

Euro-Med Intl.

FDA 510(k) clearance K854891 for KNIFE, Substantially Equivalent on 1986-05-02. Applicant: Euro-Med Intl.. Device class: 1.

Clearance details

Applicant: Euro-Med Intl.
Product code: Code EMF
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 EMF

K080133 — MOUNTABLE ENDOSCOPIC BLADE2008-03-13
K982142 — MOUNTABLE ENDOSCOPIC KNIFE1998-12-30
K890214 — MICROSURGERY RAZOR BLADE HOLDER1989-01-27
K890215 — MICROSURGICAL SCARIFIER1989-01-27
K890217 — MICROSURGICAL KNIVES1989-01-27

More clearances from Euro-Med Intl.

K883884 — PROSTATIC CORE-CUT NEEDLE1988-12-05
K882404 — KEVOR-CURETTE1988-07-08
K854890 — HOOK PROBE1986-05-02
K854894 — SPOON1986-05-02
K854895 — BASKET FORCEP1986-05-02

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