(30 days)
No
The description focuses on the physical measurement of CO2 and calculation of parameters based on these measurements, with no mention of AI or ML techniques.
No.
The device is described as a monitoring system that measures gastrointestinal CO2 and calculates related parameters, which falls under diagnostic or monitoring functions, not therapeutic intervention.
Yes
The device is intended for monitoring gastrointestinal CO2 and calculating various gastrointestinal tonometry parameters (e.g., intramucosal pH), which are measurements used to assess a patient's physiological state and help diagnose conditions.
No
The device description explicitly states it is a "single-width plug-in parameter module" and describes physical actions like filling and deflating a balloon, indicating it is a hardware component.
Based on the provided information, this device is not an In Vitro Diagnostic (IVD).
Here's why:
- IVD Definition: An IVD is a medical device intended for use in vitro for the examination of specimens, including blood, tissue, and urine, derived from the human body, to provide information for diagnostic, monitoring, or compatibility purposes.
- Device Function: The Datex-Ohmeda Tonometry module, E-TONO, directly measures gastrointestinal PCO2 (PgCO2) in vivo (within the patient's body) using a catheter placed in the stomach or intestine. It does not analyze specimens in vitro.
- Intended Use: The intended use is for "gastrointestinal tonometry measurements" and "monitoring gastrointestinal CO2 (PgCO2)" directly within the patient.
Therefore, because the device performs measurements directly within the patient's body rather than on a specimen outside the body, it does not fit the definition of an In Vitro Diagnostic.
N/A
Intended Use / Indications for Use
Intended Use:
The Datex-Ohmeda Tonometry module , E-TONO is intended to be used with Datex-Ohmeda modular monitoring systems for gastrointestinal tonometry measurements.
Indications for use:
The Datex-Ohmeda Tonometry Module is indicated for monitoring gastrointestinal CO2 (PgCO2) and calculation of various gastrointestinal tonometry parameters (gastrointestinal -arterial PCO2 difference, gastrointestinal -end-tidal PCO2 difference and intramucosal pH) when used with a Datex-Ohmeda modular monitoring system. It is indicated for use in hospital patients.
The Tonometry module is indicated for use by qualified medical personnel only.
Product codes
CCK
Device Description
The Datex-Ohmeda Tonometry module, E-TONO is a single-width plug-in parameter module for a Datex-Ohmeda modular monitoring system. The Datex-Ohmeda Tonometry module, E-TONO can be used with the following Datex-Ohmeda modular monitors:
S/5TM Anesthesia Monitor (AM), S/5TM Compact Anesthesia Monitor (CAM), S/5TM Critical Care Monitor (CCM), or S/5TM Compact Critical
Care Monitor (CCCM), with monitor software versions 99 or newer.
The tonometry module measures the gastrointestinal PCO2 (PgCO2) every 10 minutes utilizing a tonometry catheter placed into the patient's stomach or intestine. Initially the module fills the balloon of the Tonometrics catheter with ambient air, then repeatedly every 10 min deflates the balloon, analyzes and displays the PgCO2, and inflates the balloon again.
All the calculated parameters can be selected on the display, and trended. Alarms for Tonometry are taken care of by the host monitor and follow the user interface for alarms in Datex-Ohmeda S/5 patient monitors. There are auditory and visual alarms and user adjustable limits for Tonometry variables. The accessories are the same for the E-TONO module and the predicate device, the M-TONO (K993656).
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
gastrointestinal, stomach or intestine
Indicated Patient Age Range
Not Found
Intended User / Care Setting
qualified medical personnel, hospital patients
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Datex-Ohmeda S/5™ Tonometry Module, E TONO and accessories has been assessed against the standards below. The device has been thoroughly tested through validation and verification of specifications.
- COUNCIL DIRECTIVE 93/42/EEC of 14 June 1993 concerning medical devices
- FDA/DCRND Reviewer Guidance for Premarket Notification Submissions, November 1993
- IEC 60601-1:1988 + Amdt. 1:1991 + Amdt. 2:1995 (Part 1: General requirements for safety)
- EN 60601-1:1990+ A1:1993 + A13:1996 + A2:1995 (identical to IEC60601-1:1988 + Amdt. 1:1991 + Amdt. 2:1995)
- CAN/CSA C22.2 No. 601.1-M90 + S1:1994 (Canadian deviations to IEC 60601-1:1988 + Amdt. 1:1991) + S2:1998 (=IEC Amdt 2:1995)
- UL 2601-1, October 24, 1997 (U.S. deviations to IEC 60601-1:1988 + Amdt. 1:1991+ Amdt. 2:1995)
- IEC 60601-1-2:2001 (Electromagnetic compatibility Requirements and tests)
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
K992181, K993296, K983366, K980384
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 868.1400 Carbon dioxide gas analyzer.
(a)
Identification. A carbon dioxide gas analyzer is a device intended to measure the concentration of carbon dioxide in a gas mixture to aid in determining the patient's ventilatory, circulatory, and metabolic status. The device may use techniques such as chemical titration, absorption of infrared radiation, gas chromatography, or mass spectrometry.(b)
Classification. Class II (performance standards).
0
K052167
PAGE 1 OF 3
SEP - 8 2005
Page 1 of 3
Premarket Notification 510(k) Summary As required by section 807.92
Datex-Ohmeda S/5TM Tonometry Module, E TONO and accessories
GENERAL COMPANY INFORMATION as required by 807.92(a)(1)
COMPANY NAME/ADDRESS/PHONE/FAX:
GE Healthcare 86 Pilgrim Road Needham, MA 02492 USA Tel: 781-449-8685 Fax: 781-433-1344
NAME OF CONTACT:
Mr. Joel Kent
DATE:
September 1, 2005
DEVICE NAME as required by 807.92(a)(2)
TRADE NAME: Datex-Ohmeda S/5TM Tonometry Module, E TONO and accessories COMMON NAME: Regional capnometer CLASSIFICATION NAME: The following Class II classification appears applicable: Product Code Classification Name CFR Section CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-phase 868.1400
NAME OF LEGALLY MARKETED DEVICE FOR WHICH A CLAIM OF SUBSTANTIAL EQUIVALENCE IS MADE as required by 807.92(a)(3)
The Datex-Ohmeda S/5TM Tonometry Module, E-TONO is substantially equivalent in safety and effectiveness to the legally marketed (predicate) Datex-Ohmeda M-TONO Module (K993656).
Page 2 of 3
DEVICE DESCRIPTION as required by 807.92(a)(4)
The Datex-Ohmeda Tonometry module, E-TONO is a single-width plug-in parameter module for a Datex-Ohmeda modular monitoring system. The Datex-Ohmeda Tonometry module, E-TONO can be used with the following Datex-Ohmeda modular monitors:
S/5TM Anesthesia Monitor (AM), S/5TM Compact Anesthesia Monitor (CAM), S/5TM Critical Care Monitor (CCM), or S/5TM Compact Critical
Care Monitor (CCCM), with monitor software versions 99 or newer.
The tonometry module measures the gastrointestinal PCO2 (PgCO2) every 10 minutes utilizing a tonometry catheter placed into the patient's stomach or intestine. Initially the module fills the balloon of the Tonometrics catheter with ambient air, then repeatedly every 10 min deflates the balloon, analyzes and displays the PgCO2, and inflates the balloon again.
All the calculated parameters can be selected on the display, and trended. Alarms for Tonometry are taken care of by the host monitor and follow the user interface for alarms in Datex-Ohmeda S/5 patient monitors. There are auditory and visual alarms and user adjustable limits for Tonometry variables. The accessories are the same for the E-TONO module and the predicate device, the M-TONO (K993656).
1
The accessories have also been cleared separately under (K992181), (K993296), (K983366), and (K980384).
INTENDED USE as required by 807.92(a)(5)
Intended Use:
The Datex-Ohmeda Tonometry module , E-TONO is intended to be used with Datex-Ohmeda modular monitoring systems for gastrointestinal tonometry measurements.
Indications for use:
The Datex-Ohmeda Tonometry Module is indicated for monitoring gastrointestinal CO2 (PgCO2) and calculation of various gastrointestinal tonometry parameters (gastrointestinal -arterial PCO2 difference, gastrointestinal -end-tidal PCO2 difference and intramucosal pH) when used with a Datex-Ohmeda modular monitoring system. It is indicated for use in hospital patients.
The Tonometry module is indicated for use by qualified medical personnel only. SUMMARY OF TECHNOLOGICAL CHARACTERITICS OF DEVICE COMPARED
TO THE PREDICATE DEVICE as required by 807.92(a)(6)
The Datex-Ohmeda S/5TM Tonometry Module, E-TONO is substantially equivalent in safety and effectiveness to the legally marketed (predicate) Datex-Ohmeda M-TONO Module (K993656).
The E-TONO module has the following similarities compared to the predicate M-TONO (K993656):
- · identical intended use and indications for use
- · identical fundamental scientific technology
- · identical electronic measurement board
- · same module software (version changed from 1.0 to 1.1)
- · use the same operating principle
- · identical accessories
- · have the same user interface at the monitor and alarms (can be used with the same monitor software)
- · the Customer and parameter specifications are the same
- · have the same safety and effectiveness
- · are manufactured using the same processes
Page 3 of 3
The main differences between the new E-TONO and the predicate M-TON() (K993656) is primarily due to fact that the new E-TONO module has the following changes:
- · new color, shape, and size and thus differing mechanics
- The front panel and labeling have changed
- · Minor modification to module software
Based on the analysis and other documentation included in this 510(k) notification and attachments it is evident that the main features and indications for use of the Datex-Ohmeda S/5TM Tonometry Module, E-TONO are substantially equivalent to the predicate Datex-Ohmeda M-TONO Module (K993656).
SUMMARY OF NONCLINICAL TESTING FOR THE DEVICE and CONCLUSIONS as required by 807.92(b)(1)(3)
2
Datex-Ohmeda S/5™ Tonometry Module, E TONO and accessories has been assessed against the standards below. The device has been thoroughly tested through validation and verification of specifications.
- COUNCIL DIRECTIVE 93/42/EEC of 14 June 1993 concerning medical devices
- · FDA/DCRND Reviewer Guidance for Premarket Notification Submissions, November 1993
- IEC 60601-1:1988 + Amdt. 1:1991 + Amdt. 2:1995 (Part 1: General requirements for safety)
- · EN 60601-1:1990+ A1:1993 + A13:1996 + A2:1995 (identical to IEC60601-1:1988 + Amdt. 1:1991 + Amdt. 2:1995)
- · CAN/CSA C22.2 No. 601.1-M90 + S1:1994 (Canadian deviations to IEC 60601-1:1988 + Amdt. 1:1991) + S2:1998 (=IEC Amdt 2:1995)
- · UL 2601-1, October 24, 1997 (U.S. deviations to IEC 60601-1:1988 + Amdt. 1:1991+ Amdt. 2:1995)
- IEC 60601-1-2:2001 (Electromagnetic compatibility Requirements and tests)
CONCLUSION:
The summary above shows that there are no new questions of safety and effectiveness for the Datex-Ohmeda S/5TM Tonometry Module, E-TONO when compared to the legally marketed (predicate) Datex-Ohmeda M-TONO Module (K993656).
3
Image /page/3/Picture/2 description: The image shows a black and white drawing of a bird in flight. The bird is facing to the right and has its wings spread. There is text in a circular pattern around the bird. The text is not clear enough to read.
SEP - 8 2005
Food and Drug Administration 9200 Corporate Boulevard Rockville MI) 20050
Mr. Joel C. Kent Manager, Quality and Regulatory Affairs GE Healthcare 86 Pilgrim Road NEEDHAM MA 02492
Re: K052167
Trade/Device Name: Datex-Ohmeda S/5" Tonometry Module, E TONA and accessories Regulation Number: 21 CFR §868.1400 Regulation Name: Carbon dioxide gas analyzer Regulatory Class: II Product Code: CCK Dated: August 5, 2005 Received: August 9, 2005
Dear Mr. Kent:
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.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such 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); 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.
4
This letter will allow you to begin marketing your device as described in your Section 5 10(k) I his letter will anow you to begin manketing your accession of your device to a legally premarket nothication. THC PDA midnig of sacchanial of 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 if you desire specific advice for your do rout with to be of the regulation numbers, based on the regulation number at the top of this letter:
| 21 CFR 876.xxxx | (Gastroenterology/Renal/Urology) | 240-276-0115 |
|---|---|---|
| 21 CFR 884.xxxx | (Obstetrics/Gynecology) | 240-276-0115 |
| 21 CFR 892.xxxx | (Radiology) | 240-276-0120 |
| Other | 240-276-0100 |
Also, please note the regulation entitled, "Misbranding by reference to premarket notification the Also, please note the regulation entitled, "Wisolarians on your responsibilities under the Act from the 190 807.97). You may outlin other general information on J. S. J. S. J. S. S. J. S. S. Stance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Nancy C. Brogdon
Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
Indications for Use
510(k) Number (if known): K052167_____________________________________________________________________________________________________________________________________
Device Name: Datex-Ohmeda S/5™ Tonometry Module, E TONO and accessories.
Indications for use:
The Datex-Ohmeda Tonometry Module is indicated for monitoring gastrointestinal CO2 (PgCO2) and calculation of various gastrointestinal tonometry parameters (gastrointestinal - arterial PCO2 difference, qastrointestinal - end-tidal PCO2 difference and intramucosal pH) when used with a Datex-Ohmeda modular monitoring system. It is indicated for use in hospital patients.
The Tonometry module is indicated for use by qualified medical personnel only.
Over-The-Counter Use _ Prescription Use _____________________________________________________________________________________________________________________________________________________________ AND/OR (Part 21 CFR 801 Subpart D) (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Nancy C Brogdon
Page _ of _
510(k) Number
510(k) Number