K011951 · Owen Mumford, Ltd. · FMF · Aug 2, 2001 · General Hospital
Device Facts
Record ID
K011951
Device Name
EZ SYRINGE
Applicant
Owen Mumford, Ltd.
Product Code
FMF · General Hospital
Decision Date
Aug 2, 2001
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 880.5860
Device Class
Class 2
Intended Use
The hand held device is intended to aid in the self-administration of drugs from a prefilled BD Hypak 1 ml disposable glass syringe. The device incorporates enlarged wings to facilitate gripping and a semi-automatic feature to remove the needle shield of the Hypak syringe.
Device Story
EZ Syringe is a hand-held, non-sterile manual device designed to assist patients or caregivers with home self-administration of medication using 1 ml BD Hypak disposable glass pre-filled syringes. The device features enlarged wings for improved grip and a semi-automatic mechanism that removes the syringe needle shield with a single twist. It facilitates loading and unloading of the syringe. By simplifying the handling and preparation of the pre-filled syringe, the device aids patients in adhering to recommended treatment regimens, potentially increasing confidence and ease of use during manual injections.
Clinical Evidence
Bench testing only. Performance testing included parking action of the boot remover, drop testing, and environmental testing to verify correct function and reliability. User trial data indicated successful patient and caregiver preference for the device in carrying out manual injections.
Technological Characteristics
Hand-held, non-sterile manual device. Designed for 1 ml BD Hypak disposable glass pre-filled syringes. Features include front-twisting body with wings for needle shield removal and large finger grips. Mechanical operation; no energy source. No software or electronic components.
Indications for Use
Indicated for patients or caregivers in the home setting to assist in the self-administration of medication using a 1 ml BD Hypak disposable glass pre-filled syringe.
Regulatory Classification
Identification
A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.
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K111467 — FLEXI-Q DV AND DVR AUTO-INJECTORS · Elcam Medical Acal · Feb 9, 2012
K042314 — SYRINGE GRIP FOR THE AVONEX PRE-FILLED SYRINGE · Biogen · Nov 22, 2004
Submission Summary (Full Text)
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## 510(K) SUMMARY.
Submitted by:
Mr. Robert Shaw. Vice President. Owen Mumford Incorporated. 1755 - A West Oak Commons Court. Marietta. Georgia 30062. USA.
770-977-2226. Tel: Fax: 770-977-2866.
Device Name: Classification Name: Predicate Device:
EZ Syringe. Piston Syringe, Accessory, Inject-Ease (K872233).
Owen Mumford Limited has been successfully marketing syringe needle introducers throughout the world since 1986.
These products provide a safe and simple way to aid the patient in the home with a recommended treatment regime via a self-administered manual injection.
#### DEVICE DESCRIPTION.
The EZ Syringe O.T.C is a hand held, non-sterile manual device using 1 ml BD Hypak disposable glass pre-filled syringe.
The devices are designed for use with the 1 ml BD Hypak disposable glass syringe, and to accommodate self- use in the home by the patient or caregiver. The device incorporates enlarged wings to facilitate gripping and a semi-automatic feature to remove the needle shield of the Hypak syringe.
The device contains a number of features which adds to its safety and effectiveness, these are as follows :-
- Front twisting body with wings which easily removes the soft needle shield from the . syringe.
- Large finger grip engineered to aid in the handling of the device. �
- Allows the pre-filled syringe to be loaded and unloaded. �
- Requires one turn to remove the needle shield. �
510(K) Submission EZ Syringe. June 2001 -
{1}------------------------------------------------
## INTENDED USE.
The hand held device is intended to aid in the self-administration of drugs from a prefilled BD Hypak 1 ml disposable glass syringe. The device incorporates enlarged wings to facilitate gripping and a semi-automatic feature to remove the needle shield of the Hypak syringe.
## OPERATIONAL.
The design concepts of the EZ Syringe submitted in this application are such that it makes the principal quite basic in its function to aid the patient in the home to support a manual injection.
### PERFORMANCE.
A number of tests have been performed proving the correct action of a wide range of functions for the EZ Syringe, they are:-
- · Parking Action of Boot Remover.
- · Drop Test.
- Environmental .
The performance testing completed under section 6 of this 510(K) submission indicates that the device performs within the agreed specification and is safe and reliable.
#### USER TRIAL.
The correspondence included in section 9 of this over - the - counter submission clearly indicates the success of the device for patient or carer preference for carrying out a manual injection.
510(K) Submission. EZ Syringe. June 2001.
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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three stripes forming its body and wings. The eagle is enclosed in a circle, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is written around the circle's perimeter. The text is in all caps and is arranged to follow the curve of the circle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
AUG - 2 2001
Mr. Robert Shaw Vice President Owen Mumford, Limited 1755 A West Oak Commons Court Marietta, Georgia 30062
Re : K011951 Trade/Device Name: EZ Syringe 880.5860 Requlation Number: Regulatory Class: II Product Code: FMF Dated: June 21, 2001 Received: June 21, 2001
Dear Mr. Shaw:
We have reviewed your Section 510(k) notification of intent to we have reviewed your beoced above and we have determined the market the device forline.com (for the indications for use stated in the enclosure) to legally marketed predicate use stated in the cholobars, e commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to the enactment acco on reclassified in accordance with the devices that have Federal Food, Drug, and Cosmetic Act (Act), provisions of the reachar room, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual provisions of the ing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may (Special Concrois) additional controls. Existing major be subject to bacting your device can be found in the Code of Fegulations arrooms, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with Subscuncially Squarenting Practice requirements, as set ene Current Souality System Regulation (QS) for Medical Forch in the gas gaint (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug chrough periodre go mapleverify such assumptions. Failure to nomiliberation of regulation may result in regulatory In addition, FDA may publish further announcements action. concerning your device in the Federal Register. Please note:
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Page 2 - Mr. Shaw
this response to your premarket notification submission does this response to your premazio got have under sections 531 not afrect any obligation you mees under the Electronic through 542 of the net 102 xevisions, or other Federal laws or requlations.
This letter will allow you to begin marketing your device as This lecter will arrow yourse researce notification. The FDA described in your 510(x) providence of your device to a legally I inding of substancial equice in a classification for your marketed predicate device robated in the market.
If you desire specific advice for your device on our labeling II you desire bpccirie and additionally 809.10 for in regulation (ar endevices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on Compilance at (501) 5927 5927 device, please contact the Dromocion and adversions (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 807.97). Other general premation on your responsibilities under the Act may be Information on your responsible of Small Manufacturers Assistance oblained from the bivibies. (800) 638-2041 or (301) 443-6597 or at its internet address
"http://www.fda.gov/cdrh/dsma/dsmamain.html".
Sincerely Yours,
Timothy A. Ulatowski
Timo Director Division of Dental, Infection Control and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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(Unknown). 510(K) Number:
EZ - Syringe O. T. C. Device Name:
Indications for Use:
The hand held device is intended to aid in the self-administration of drugs from a prefilled BD Hypak 1 ml disposable glass syringe. The device incorporates entarged wings
filled BD Hypak 1 ml disposable glass syringe. The device incorporated wings Inted BD Hypak I ini disposure grass by ago ago remove the needle shield of the Hypak syringe.
# (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PACE IF NEEDED)
Concurrence of the CDRA, Office of Evaluation (ODE)
Prescription Use: ............................................................................................................................................................ (Per 21 CFR 801.109)
**Over-The-Counter Use:**..................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................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Laura Cucciariale
(Division Sign-Off) Division of Dental, Infection Control, and General Hospital Devices
510(k) Number
510(K) Submission. EZ Syringe. June 2001.
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