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Results for “Model 4000”
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177 devices found
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Model 4000
UDI-DI 35099169402462
Vitalograph Ireland, Ltd.
·
,
Ireland
(FDA 510(k) applicant)
Class II
GUDID
on market
None
GUDID
II
111 variants
Model 4000
4000
UDI-DI 05099169400382
Withdrawn
Model 4000
4000
UDI-DI 05099169402423
Model 4000
4000
UDI-DI 05099169402515
Model 4000
4000
UDI-DI 05099169403574
Withdrawn
Model 4000
4000
UDI-DI 05099169407039
Model 4000
4000
UDI-DI 05099169407480
Withdrawn
Model 4000
4000
UDI-DI 35099169402011
Model 4000
4000
UDI-DI 35099169402486
Model 4000
4000
UDI-DI 35099169402684
Model 4000
4000
UDI-DI 35099169402783
Model 4000
4000
UDI-DI 35099169402912
See all variants of this device
Baby Dopplex 4000, Model Bd 4000
Huntleigh Healthcare Limited
·
,
FDA registration: United States
Class II
FDA 510(k)
K990569
Active
Cleared 24 Jan 2000
Active
510(k)
510(k)
II
Pc Compatible Blood Pressure Monitor, Model Ak-4000TU, Bp-410U, Bp-410R; Automatic Digital Wrist Blood Press. Monitor.
Ya Horng Electronic Co., Ltd.
·
,
Taiwan
Class II
FDA 510(k)
K051862
Active
Cleared 23 Aug 2005
Active
510(k)
510(k)
II
Models 4000S & 4000S/L
Adr Ultrasound
·
,
FDA registration: United States
Class II
FDA 510(k)
K813543
Active
Cleared 24 Feb 1982
Active
510(k)
510(k)
II
Amluck Ya Horng Pc Compatible Wrist Blood Pressure Monitor, Model Ak-4000T
Ya Horng Electronic Co., Ltd.
·
,
Taiwan
Class II
FDA 510(k)
K040528
Active
Cleared 15 Apr 2004
Active
510(k)
510(k)
II
Patient Monitor, Models Dash 3000, 4000 And 5000
Open recall
Ge Medical Systems Information Technologies
·
,
FDA registration: United States
Class II
FDA 510(k)
K051367
Active
Cleared 20 Jun 2005
Active
510(k)
510(k)
II
Models 4000, 4900, 6000, 8000, 8900, Luxus 60, 100&1700
Heraeus Lasersonics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K902061
Active
Cleared 10 Jul 1990
Active
510(k)
510(k)
II
Cirrus Hd-Oct, Model 4000
Carl Zeiss Meditec, Inc.
·
,
United States
Class II
FDA 510(k)
K063378
Active
Cleared 26 Jan 2007
Active
510(k)
510(k)
II
Defender Room Air Cleaner, Model Rac-4000A
Hmi Industries, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K010616
Active
Cleared 28 Mar 2001
Active
510(k)
510(k)
II
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