VASOVAPOR

K101320 · Lexion Medical, LLC · HIF · Jun 24, 2010 · Obstetrics/Gynecology

Device Facts

• Record ID: K101320
• Device Name: VASOVAPOR
• Applicant: Lexion Medical, LLC
• Product Code: HIF · Obstetrics/Gynecology
• Decision Date: Jun 24, 2010
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 884.1730
• Device Class: Class 2

Intended Use

VasoVapor™ is a gas conditioner accessory device for use in endoscopic vessel harvesting surgical procedures, intended to heat, humidify and filter a CO2 gas stream for insufflation of the surgical cavity.

Device Story

VasoVapor™ is a single-use accessory for laparoscopic insufflators. It receives regulated CO2 gas from an insufflator, passes it through an in-line filter, and then through a cassette containing a heating element and humidification media. The conditioned gas is delivered via a Luer lock connector to an insufflation needle or trocar for entry into the patient's surgical cavity. The device includes a control module housing safety and control circuits. It is used in clinical settings during endoscopic vessel harvesting procedures. By warming and humidifying the CO2, the device aims to improve conditions within the surgical cavity.

Clinical Evidence

No clinical data provided. Substantial equivalence is supported by bench performance testing and comparison to predicate devices.

Technological Characteristics

Single-use disposable filter, heater, and humidifier tubing set with a control module. Operates by heating and humidifying a CO2 gas stream. Connects to standard insufflator outlet ports via Luer lock. Includes control and safety circuits.

Indications for Use

Indicated for use in endoscopic vessel harvesting surgical procedures to heat, humidify, and filter CO2 gas for insufflation of the surgical cavity.

Regulatory Classification

Identification

A laparoscopic insufflator is a device used to facilitate the use of the laparoscope by filling the peritoneal cavity with gas to distend it.

Predicate Devices

• Insuflow® (K063546)
• Insuflow® (K090456)

Submission Summary (Full Text)

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K101 320
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# SECTION 2. SUMMARY AND CERTIFICATION

JUN 2 4 2010

## A. 510(K) SUMMARY

### Summary of Safety and Effectiveness

In accordance with 21 CFR 807.92, the following information constitutes the summary of safety and effectiveness for VasoVapor™

| SUBMITTER'S NAME: | LEXION Medical LLC |
|---------------------|-----------------------|
| ADDRESS: | 5000 Township Parkway |
| | St. Paul, MN 55110 |
| CONTACT PERSON: | Bernard (Bud) Horwath |
| TELEPHONE NUMBER: | 651-361-8041 |
| FAX NUMBER: | 651-351-8001 |
| DATE OF SUBMISSION: | 7 May 2010 |

#### 1. Identification of device

Proprietary Name: VasoVapor™ Common Name: Laparoscopic Insufflator Gas Conditioner Classification Status: Class II per regulations 884.1730 Product Code: HIF

#### 2. Equivalent devices

LEXION Medical believes that VasoVapor™ is substantially equivalent to the following devices:

Insuflow®, K063546
Insuflow®, K090456

Vaso Vapor™ is the same gas conditioner insufflator accessory device as cleared under 510(k) K063546 and K090456 and has a subset of the intended use of the predicate device cleared under 510(k) K090456.

### 3. Description of the Device

The VasoVapor™ device is a single use device that attaches to the outlet port of an insufflator or other regulated CO2 source and is designed to warm and humidify the CO2 gas stream prior to insufflation into the surgical cavity. The Vaso Vapor™ device consists of a disposable filter heater/humidifier tubing set and a control module that houses the control and safety circuits for the system.

Regulated CO2 gas flows into the VasoVapor™ device, through the in-line filter, continues along the tube to enter the VasoVapor™ device cassette that contains the heating element and humidification media, through a tube that connects via a Luer lock connector to a gas entrance port or an insufflation needle/trocar and finally flows into the patient's surgical cavity.

LEXION Medical VasoVapor™ 510k

### Confidential

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#### 4. Intended use

VasoVapor™is a gas conditioner accessory device for use in endoscopic vessel harvesting surgical procedures, intended to heat, humidify and filter a CO2 gas stream for insufflation of the surgical cavity.

#### ડ. Technological characteristics, comparison to predicate device.

Technically, the VasoVapor™ is identical to the Insuflow cleared for market in 510(k) K063546 and K090456. The indications for use for the VasoVapor™ are patterned affer the predicate devices, being specific to the endoscopic vessel harvesting application.

#### 6. Discussion of performance testing.

Extensive performance testing has been conducted to assure that the VasoVapor™ (i.e., Insuflow ) performs in accordance with its specifications and applicable standards. Details of that testing were provided in 510(k) K063546 and K090456 are referenced in Section 5 for completeness.

#### 7. Conclusion

Based on a comparison to the predicate devices, it is the conclusion of LEXION Medical that VasoVapor™ is substantially equivalent to devices already on the market being used for this application (cleared by the 510(k) process) and presents no new concerns about safety and effectiveness.

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Image /page/2/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract image of an eagle.

Food and Drug Administration 10903 New Hampshire Avenue Document Mail Center - WO66-G609 Silver Spring, MD 20993-0002

### JUN 2 4 2010

Mr. Bernard (Bud) Horwath Regulatory Consultant LEXION Medical LLC 5000 Township Parkway ST PAUL MN 55110

Re: . K101320

> Trade Name: VasoVapor™ Regulation Number: 21 CFR §884.1730 Regulation Name: Laparoscopic insufflator Regulatory Class: II Product Code: HIF Dated: May 7, 2010 Received: May 11, 2010

Dear Mr. Horwath:

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 Medical 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

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); medical device reporting of medical device-related

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adverse events) (21 CFR 803); good manufacturing practice requirements as set 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.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

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/MedicalDevices/Resourcesfor You/Industry/default.htm.

Sincerely yours,

Janine M. Morris

Acting Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# B. INDICATIONS FOR USE

510(k) Number K10 | 320

Device Name: VasoVapor™

### Indications for Use:

VasoVapor™ is a gas conditioner accessory device for use in endoscopic vessel harvesting surgical procedures, intended to heat, humidify and filter a CO2 gas stream for insufflation of the surgical cavity.

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Concurrence of CDRH, Office of Device Evaluation (ODE)

Prescription Use Over the Counter Use X OR (Per 21 CFR 801.109) vision Sign=Off on of ReBroductive, Abdominal, and ales Devia LEXION Medical VasoVapor™ 510k

Confidential

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