PHASE I CURETTE— 510(k) K935822

Substantially Equivalent

Phase I Corp.

FDA 510(k) clearance K935822 for PHASE I CURETTE, Substantially Equivalent on 1994-04-28. Applicant: Phase I Corp.. Device class: 1.

Clearance details

Applicant: Phase I Corp.
Product code: Code HCY
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1993-12-03
Decision date: 1994-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HCY

K980096 — OAC (OPTICAL ASPIRATING CURETTE)1998-05-01
K944238 — ENDOCYTE TM1995-09-15
K901442 — BAXTER D & C TRAY1990-07-26
K890384 — UTERINE CURETTE1989-02-13
K881794 — IVORY FINDER SET1988-07-08

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