Welch Allyn #48100 Task Lite W/Accessories AS List

FDA 510(k) K852949 · Welch Allyn, Inc.

Substantially Equivalent

510(k) numberK852949

Submission

Device name
Welch Allyn #48100 Task Lite W/Accessories AS List
Applicant
Welch Allyn, Inc.
Skaneateles Falls, NY, US
Received
July 11, 1985
Decision date
September 4, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

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)DeviceApplicantDecision
K954943NevoscopeKZF · Traditional Nizar A. Mullani03/27/1996SE
K952835Welch Allyn Video EpiscopeKZF · Traditional Welch Allyn, Inc.09/22/1995SE
K945507H 5100, H 5200, H 5300KZF · Traditional Rudolf Riester GmbH & Co. KG12/09/1994SE
K941869Splint, Pneumatic, Arm & Splint, Pneumatic, LegKZF · Traditional The Lighthouse For the Blind, Inc.08/03/1994SE
K936088Wave Fluorescent MagnifierKZF · Traditional Burton Medical Products Corp.04/26/1994SE
K940284Meddev Multarray Medical Examining Light ModificationKZF · Traditional Meddev International Corp.02/28/1994SE
K933564Skytron Exam LightKZF · Traditional Skytron, Div. the Kmw Group, Inc.02/10/1994SE
K935832ChromophareKZF · Traditional Berchtold Holding GmbH02/03/1994SE
K934259Ac-Powered Medical Examination LightKZF · Traditional Welch Allyn, Inc.01/28/1994SE
K932719Ritter Model 158 and 159 Exam LightsKZF · Traditional Midmark Corp.12/02/1993SE

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K171621Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System…MHX · Special 06/30/2017SE
K142356Connex Spot Monitor,901058 Vital Signs Monitor CoreMWI · Traditional 12/19/2014SE
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Questions and answers

When was Welch Allyn #48100 Task Lite W/Accessories AS List cleared by the FDA?

Welch Allyn #48100 Task Lite W/Accessories AS List (K852949) received a 510(k) decision of Substantially Equivalent on September 4, 1985, 55 days after the submission was received.

What is the product code of K852949?

The FDA product code is KZF – Device, Medical Examination, Ac Powered, a Class I (low risk) device regulated under 21 CFR 880.6320.