RANDALL CURETTE— 510(k) K854888

Substantially Equivalent

Euro-Med Intl.

FDA 510(k) clearance K854888 for RANDALL CURETTE, Substantially Equivalent on 1985-12-24. Applicant: Euro-Med Intl.. Device class: 1.

Clearance details

Applicant: Euro-Med Intl.
Product code: Code FZS
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-12-06
Decision date: 1985-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danville, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FZS

K932493 — SURGICAL CURETTE1994-01-07
K902000 — KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD1990-08-21
K892521 — CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE1989-05-01
K891888 — CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPER1989-04-12
K891334 — ACU-CURETTE1989-04-11

More clearances from Euro-Med Intl.

K883884 — PROSTATIC CORE-CUT NEEDLE1988-12-05
K882404 — KEVOR-CURETTE1988-07-08
K854890 — HOOK PROBE1986-05-02
K854891 — KNIFE1986-05-02
K854894 — SPOON1986-05-02

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