CHROMOPHARE D500, D530, D650

K991527 · Berchtold Holding GmbH · FSY · May 27, 1999 · General, Plastic Surgery

Device Facts

• Record ID: K991527
• Device Name: CHROMOPHARE D500, D530, D650
• Applicant: Berchtold Holding GmbH
• Product Code: FSY · General, Plastic Surgery
• Decision Date: May 27, 1999
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 878.4580
• Device Class: Class 2

Intended Use

The Surgical lights CHROMOPHARE® D500, D630 and D650, are intended to illuminate locally the operating site on the patient's body with a high intensity, shadow free, "cold" light.

Device Story

CHROMOPHARE D Series (D500, D530, D650) are ceiling-mounted surgical lights providing high-intensity (85,000 to 150,000 lux), shadow-free, "cold" illumination. Designed for use in operating rooms by surgeons and clinical staff. Features include lamp failure switching, optional CCD-video camera integration (D530/D650), and "EndoLite" version for endoscopy. System integrates with Berchtold Hermes OR Control Center, allowing physicians to adjust light settings via wall-mounted touch panels or voice-activated controls, reducing reliance on verbal communication during surgery. Benefits include improved visualization and simplified control of the surgical environment.

Clinical Evidence

Bench testing only; compliance with IEC 601 and UL 544 safety standards.

Technological Characteristics

Ceiling-mounted surgical light system; intensity 85,000-150,000 lux; shadow-free "cold" light technology; optional CCD-video camera; integration with Hermes OR Control Center via touch panel/voice control; meets IEC 601 and UL 544 safety standards.

Indications for Use

Indicated for illumination of the operating site on a patient's body during surgical procedures.

Regulatory Classification

Identification

A surgical lamp (including a fixture) is a device intended to be used to provide visible illumination of the surgical field or the patient.

Special Controls

*Classification.* Class II (special controls). The device, when it is an operating room lamp, a surgical instrument light, a surgical floor standing light, an endoscopic surgical light, a surgical light connector, a ceiling mounted surgical light, a surgical light carrier, surgical light accessories, a surgical lamp, a remote illuminator, or an incandescent surgical lamp, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 878.9.

Predicate Devices

• CHROMOPHARE D659 (K965130)

Submission Summary (Full Text)

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MAY 27 1999

K991527

### 8.0 510(k) SUMMARY

As Required By 21 CFR 807.92

Submitter:

Berchtold GmbH & Co Ludwigstaler Str. 25 D-78532 Tuttlingen Germany

0049 7461 181-0 Phone number: 0049 7461 181-100 Fax number:

Wolfram K. Hill Contact person: Manager R & D

Device Name:

Trade Name:

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一

Classification name: Product code: Device class:

CHROMOPHARE® D500 CHROMOPHARE® D530
CHROMOPHARE® D650 Light, Surgical, Ceiling Mounted FSY Class II

Device Description:

Devilos collection CHROMOPHARE® D Series lights are suitable for all types of surgical
The light The Berchtold CHROMOPHARE® D Senes lights and "colder" light stypes that gold" of the light
procedures and offers the physician a natural (whiter) and "colder" light procedures and oners the phycloids. In a continue.

Quality is series lights provides a lights provides a light intensity from 85000lx up to 150000 lux.

The light incorporates easy-to-operate switching on the second lamp
The light of failure of the main leasy to exchange lamp cartidge. Frith le The light incorporates easy-to-perate switch easy to exchange lamp carridge. For the light in case of failler. For the available of failling of the main in case of failure of the main amp and an easy to exchange later available
CHROMOPHARE® D650 and D530 is also an optional CCD-video camera available CHROMOPHARE® D650 and D530 is also an option. The light could be and a special version with "EndoLite" for endoscopical wonline of Control Control Control Control Control Control Control Control Control combined with other Berchtold lights and the Hermes Ort Some - Sense - See in the EC
Motion, Inc. The light has been designed to and meets the requirements of the IEC
. Motio 601 and UL 544 regulation for safety.

#### Intended Use:

The intent of the CHROMOPHARE® D650 is to illuminate locally the operating site on
t of the Kesked on the a bigh intensiby, shadow free, "cold" light, Light functions could The intent of the CHROMOPHARE "Dost is to thinkling tour light functions could
the patient's body with a high intensity, shadow free, "cod" light functions could the patient's body with a nigh mieristiy, stitacow libe, The HERMES .
be controlled by touch panel mounted at the wall box. The HERMES .
The controlled by accuracy in the ou be controlled by touch panel mounted at the wall being voice-activated control
OR Control Center provide the surgeon with the option with the so allow for OR Control Center provide the surged with the Option of this is to allow for
of the settings and adjustments of the CHROMOPHARE® D650. This is to allow for of the settings and adjustments of the Light settings by the physician, thereby
simplified and more direct control of the Light settings between the su simplifed and more direct control of the Light security of the pryson the surgeon
eliminating the necessity of relying upon verbal communications begined Light. eliminating the necessity of relying upon verbal ochinemation in the Surgical Light

#### Substantial Equivalence:

The CHROMOPHARE® D650 described in this submission is substantially equivalent to The CHROMOPHARE® D659 described in K965130. Any difference that exists has no the CHROMOPHARE" Doss described in though enhances the usefulness in the negative effect on safety of the medical supply units, as indicated above, has been
chosen application. Safety of the medical supply units, as indicated above, has been
t the chosen application. Salely of the medical ouppy."
established by meeting the requirements of IEC 601 and UL 544.

Image /page/0/Picture/22 description: The image shows the logo for Berchtold. The logo consists of the word "BERCHTOLD" in a sans-serif font, followed by two vertical lines and a solid black circle. The circle has a small "®" symbol to the right of it.

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Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

MAY 27 1999

Mr. Wolfram K. Hill Manager, Research and Development Berchtold GmbH & Co. Ludwigstaler Str. 25 Postfach 4052 D-78505 Tuttlingen Germany

K991527 Re:

Trade Name: Chromophare D500, D530, D530, D650 Regulatory Class: II Product Code: FSY Dated: April 28, 1999 Received: May 3, 1999

Dear Mr. Hill:

We have reviewed your Section 510(k) notification of intent to market the device referenced We have reviewed your Section 510(x) notined.com tially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate comments as to de use stated in the enclosure) to devices manages in the Medical Devices that May 28, 1976, the enaculient date of the Meersal of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls Cosmetic Act (Act). You may, therefore, market the actively and the Act include requirements for provisions of the Act. The general cona of proufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III If your device is classified (see above) into such additional controls. Existing major (Premarket Approval), It may be subject to satis atist stired Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Faris 600 to 697. A substaintain'y equirement, as set forth in the Quality System Current Good Manufacturing Practices: General regulation (21 CFR Part 820) and that, Regulation (QS) for Medical Devices: Sood and Drug Administration (FDA) will verify turough periodic (QS) inspections) in the GMP regulation may result in regulatory such assumptions. Fallure to comply with the SHF regulants concerning your device in the Federal Register. Please note: this response to your premarket notification submission does Federal Register. Trease note: this response to 70 through 542 of the Act for not affect any obligation you might have under society of the Food of the Federal laws or regulations.

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# Page 2 - Mr. Wolfram K. Hill

This letter will allow you to begin marketing your device as described in your 510(k)
. The substantial and me TDA finding of substantial equivalence of your device to This letter will allow you to begin marketing your device as usefice as user as a contracted to a
premarket notification. The FDA finding of substitisation for your device a premarket notification. The Finding of substantial equivalence of your device and thus, permits
Iegally marketed predicate device results in a classification for your device your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801
Press and the contraction in adjustic devices), please contact the Office of If you desire specific advice for your device on our laboring regantset the Office of
and additionally 809.10 for in vitro diagnostic devices), please constitution and and additionally 809.10 for in nitro diagnosic devices); productions on the promotion and Compliance at [phone]. please contact the Office of Compliance at [phone].
advertising of your device, please contact the Office of Compliance at [phone] advertising of your device, please contact the Originating by reference to premarket.
Also, please note the regulation entitled, "Misbranding by reference to premarket Also, please note the regulation entitled, "Misoration on your responsibilities under the
notification" (21 CFR 807.97). Other general information on your responsibilities u notification" (21 CFR 807.97). Other general miorination on your roped.
Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free
s and be one Act may be obtained from the Division of Similar of Sincernet address
number [phone] or [phone] or at its internet address
1977 [phone] or [phone] "http://www.fda.gov/cdrh/dsmamain.html".

Sincerely yours,

Celia M. Witten, Ph.D., M.D.
Director
Division of General and
Restorative Devices
Office of Device Evaluation
Center for Devices and
Radiological Health

V

Enclosure

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## 4.0 Indication for Use

The Surgical lights CHROMOPHARE® D500, D630 and D650, are intended to illuminate locally the operating site on the patient's body with a high intensity, shadow free, "cold" light.

Wolfram Her

Nolfram Hill Manager K&D Berchtold GmbH & Co.

May 19, 99
Date

K 99152Y
510(k) Number

**Prescription Use**
(Per 21 CFR 801.109)

(Division Sign-Off) Division of General Restorative Devices 510(k) Number

S

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