PERIFIX CATHETER CONNECTOR

K033952 · B.Braun Medical, Inc. · CAZ · Feb 4, 2004 · Anesthesiology

Device Facts

• Record ID: K033952
• Device Name: PERIFIX CATHETER CONNECTOR
• Applicant: B.Braun Medical, Inc.
• Product Code: CAZ · Anesthesiology
• Decision Date: Feb 4, 2004
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 868.5140
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

A connection device used to provide various anesthetic and fluid administration devices with a single, common access point to 20 - 24 gauge Perifix catheter for delivery of anesthetics. The connector is used in conjunction with 20 - 24 gauge Perifix catheters for continuous administration of anesthetic agents.

Device Story

Perifix Catheter Connector is a mechanical device used to link anesthesia conduction catheters (epidural or nerve block) to luer-compatible fluid administration devices. It features a luer end, threading hole, compressible catheter channel, and hinged clamp mechanism. Used in clinical settings by healthcare providers during anesthesia procedures to provide a common access point for continuous anesthetic delivery. The device facilitates secure connection between the catheter and the delivery system, ensuring consistent fluid administration.

Clinical Evidence

Bench testing only.

Technological Characteristics

Mechanical connector; 1.77 inches long, 0.43 inches diameter; includes luer interface, threading hole, compressible catheter channel, and hinged clamp. Materials include a reformulated component for the catheter channel.

Indications for Use

Indicated for patients requiring continuous administration of anesthetic agents via 20-24 gauge Perifix catheters (epidural or nerve block).

Regulatory Classification

Identification

An anesthesia conduction kit is a device used to administer to a patient conduction, regional, or local anesthesia. The device may contain syringes, needles, and drugs.

Predicate Devices

• Perifix Catheter Connector (K022019)

Reference Devices

• Perifix Catheter Connector (K032144)

Submission Summary (Full Text)

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K033952

FEB - 4 2004

## 7.0 510(k) Summary

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| SUBMITTER: | B. Braun Medical Inc.<br>901 Marcon Boulevard<br>Allentown, PA 18109-9341<br>[phone], ext. 2597<br>Contact: Amy Smith, RA Specialist |
|---------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| DEVICE NAME: | Perifix® Catheter Connector |
| COMMON OR USUAL<br>NAME: | Anesthesia Catheter Connector |
| DEVICE<br>CLASSIFICATION: | Class II per Code of Federal Regulations, Title 21, § 868.5120 -<br>Anesthesia Conduction Catheter, 868.5140 - Anesthesia<br>Conduction Catheter Kit |
| PREDICATE DEVICE: | B. Braun Medical Inc.; Perifix Catheter Connector; K022019 |
| DESCRIPTION: | The Perifix Catheter Connector is a connecting device used to<br>connect an anesthesia conduction catheter (most commonly an<br>epidural or nerve block catheter) to a luer device for the<br>administration of anesthetic fluids. Catheter connectors are<br>commonly used in epidural anesthesia kits and nerve block kits.<br><br>The Perifix Catheter Connector will be available in two different<br>configurations. The first configuration is the one cleared in 510(k)<br>K022019. The second configuration is cleared in the 510(k)<br>K032144. This 510(k) submission is to expand the indications for<br>use for the first configuration to include the 24 Ga. Perifix catheter.<br><br>The Perifix Catheter Connector is approximately 1.77 inches long<br>and 0.43 inches in diameter. The connector consists of a luer<br>device on one end for the attachment of a mating luer device, a threading hole, compressible catheter channel and hinged clamp mechanism. |
| INTENDED USE: | A connection device used to provide various anesthetic and fluid<br>administration devices with a single, common access point to 20 -<br>24 gauge Perifix catheter for delivery of anesthetics. The<br>connector is used in conjunction with 20 - 24 gauge Perifix<br>catheters for continuous administration of anesthetic agents. |

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## SUBSTANTIAL EQUIVALENCE:

The Perifix® Catheter Connector indications for use cleared in K022019 are being revised to include use with a 24 Ga. Perifix catheter. The only change to this device is a change to the material of the compressible catheter channel. This change was made due to a reformulation by the supplier. This minor change does not raise any new issucs of safety or efficacy.

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Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

FEB - 4 2004

B. Braun Medical Incorporated Amy Smith, RAC Regulatory Affairs Specialist MFG. DIV. 901 Marcon Boulevard Allentown, Pennsylvania 18109-9341

Re: K033952

Trade/Device Name: Perifix Catheter Connector Regulation Number: 868.5140 Regulation Name: Anesthesia Conduction Kit Regulatory Class: II Product Code: CAZ, BSO Dated: December 19, 2003 Received: December 22, 2003

Dear Ms. Smith:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medica Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing 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 (PMA), it may be subject to such additional controls. Existing major regulytions affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 8010 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register

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Page 2 - Ms. Smith

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807): labeling (21 CFR Part 801); good manufacturing practice requirements as sct forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801). please contact the Office of Compliance at [phone]. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html

Sincerely yours,

Chuls

Chiu Lin, Ph.D. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosurc

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## 2.0 Indications for Use Statement

Page _________________________________________________________________________________________________________________________________________________________________________

510(k) Number (if known):

Perifix® Catheter Connector Device Name:

Indications For Use:

A connection device used to provide various anesthetic and fluid administration devices with a single, common access point to 20 - 24 gauge Perifix catheter for delivery of anesthetics. The connector is used in conjunction with 20 - 24 gauge Perifix catheters for continuous administration of anesthetic agents.

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Concurrence of CDRH, Office of Device Evaluation (ODE)

Prescription Use (Per 21 CFR 801.109)

Over-The-Counter Usc

sAM

(Division Sign-Off) (Division of Anesthesiology, General Hospital Infection Control, Dental Device

510(k) Number: K033752

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