Ac-Powered Medical Examination Light
FDA 510(k) K934259 · Welch Allyn, Inc.
510(k) numberK934259
Submission
- Device name
- Ac-Powered Medical Examination Light
- Applicant
- Welch Allyn, Inc.
Skaneateles Falls, NY, US - Received
- August 31, 1993
- Decision date
- January 28, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KZF – Device, Medical Examination, Ac Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6320
- Specialty
- General Hospital
Other 510(k)s with product code KZF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K954943 | NevoscopeKZF · Traditional | Nizar A. Mullani | 03/27/1996SE |
| K952835 | Welch Allyn Video EpiscopeKZF · Traditional | Welch Allyn, Inc. | 09/22/1995SE |
| K945507 | H 5100, H 5200, H 5300KZF · Traditional | Rudolf Riester GmbH & Co. KG | 12/09/1994SE |
| K941869 | Splint, Pneumatic, Arm & Splint, Pneumatic, LegKZF · Traditional | The Lighthouse For the Blind, Inc. | 08/03/1994SE |
| K936088 | Wave Fluorescent MagnifierKZF · Traditional | Burton Medical Products Corp. | 04/26/1994SE |
| K940284 | Meddev Multarray Medical Examining Light ModificationKZF · Traditional | Meddev International Corp. | 02/28/1994SE |
| K933564 | Skytron Exam LightKZF · Traditional | Skytron, Div. the Kmw Group, Inc. | 02/10/1994SE |
| K935832 | ChromophareKZF · Traditional | Berchtold Holding GmbH | 02/03/1994SE |
| K932719 | Ritter Model 158 and 159 Exam LightsKZF · Traditional | Midmark Corp. | 12/02/1993SE |
| K924447 | VitapenKZF · Traditional | Vitajet Corp. | 09/27/1993SE |
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| K212473 | Welch Allyn Connex Central StationMWI · Traditional | 10/28/2022SE |
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| K171621 | Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System…MHX · Special | 06/30/2017SE |
| K142356 | Connex Spot Monitor,901058 Vital Signs Monitor CoreMWI · Traditional | 12/19/2014SE |
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Questions and answers
When was Ac-Powered Medical Examination Light cleared by the FDA?
Ac-Powered Medical Examination Light (K934259) received a 510(k) decision of Substantially Equivalent on January 28, 1994, 150 days after the submission was received.
What is the product code of K934259?
The FDA product code is KZF – Device, Medical Examination, Ac Powered, a Class I (low risk) device regulated under 21 CFR 880.6320.