ASPIRETTE ENDOCERVICAL ASPIRATOR— 510(k) K895403

Substantially Equivalent

Unimar, Inc.

FDA 510(k) clearance K895403 for ASPIRETTE ENDOCERVICAL ASPIRATOR, Substantially Equivalent on 1989-11-29. Applicant: Unimar, Inc.. Device class: 2.

Clearance details

Applicant: Unimar, Inc.
Product code: Code HFC
Device class: Class 2
Regulation: 21 CFR 884.1050
Advisory panel: Obstetrics/Gynecology
Date received: 1989-09-07
Decision date: 1989-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilton, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HFC

K974032 — ROCKET MUCUS SAMPLER SYRINGE, STERILE, ROCKET MUCUS SAMPLER SYRINGE, CLINICALLY ASPIRATOR1997-12-22
K960263 — CERVICAL MUCOUS ASPIRATION CATHETER1996-08-29
K954903 — PEDI VAGINAL ASPIRATOR1996-04-29
K954102 — SELECTMUCUS1995-11-21
K902242 — ENDOCERVICAL ASPIRATOR1990-10-09

More clearances from Unimar, Inc.

K932432 — KRONNER REINFORCING STYLETTE1994-04-12
K920803 — HSG TRAY1992-10-19
K910317 — UNI-SEM(TM)1991-05-01
K904473 — KRONNER MANIPUJECTOR1990-12-14
K895659 — HUI MINI-FLEX1989-12-19

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