Cleared Traditional

K954102 - SELECTMUCUS
(FDA 510(k) Clearance)

K954102 · Select Medical Systems, Inc. · Obstetrics & Gynecology
Nov 1995
Decision
82d
Days
Class 2
Risk

K954102 is an FDA 510(k) clearance for the SELECTMUCUS, a Aspirator, Endocervical (Class II — Special Controls, product code HFC), submitted by Select Medical Systems, Inc. (Williston, US). The FDA issued a Cleared decision on November 21, 1995, 82 days after receiving the submission on August 31, 1995. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.1050.

Submission Details

510(k) Number K954102 FDA.gov
FDA Decision Cleared SESE
Date Received August 31, 1995
Decision Date November 21, 1995
Days to Decision 82 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF

Device Classification

Product Code HFC — Aspirator, Endocervical
Device Class Class II — Special Controls
CFR Regulation 21 CFR 884.1050

Similar Devices — HFC Aspirator, Endocervical

All 10
ROCKET MUCUS SAMPLER SYRINGE, STERILE, ROCKET MUCUS SAMPLER SYRINGE, CLINICALLY ASPIRATOR
K974032 · A & A Medical, Inc. · Dec 1997
CERVICAL MUCOUS ASPIRATION CATHETER
K960263 · Cook Urological, Inc. · Aug 1996
PEDI VAGINAL ASPIRATOR
K954903 · Cook Urological, Inc. · Apr 1996
ENDOCERVICAL ASPIRATOR
K902242 · Innovative Medical Products, Inc. · Oct 1990
O. B. PACK IV
K902032 · Customed, Inc. · Sep 1990
OBER2 MONITOR, EYE MOVEMENT (OPHTHALMIC)
K902954 · Permobil AB · Aug 1990