Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
1 active
Filters
1 active
Registry
EUDAMED
FDA 510(k)
16
FDA PMA
GUDID
14
Country / market
United States
30
Risk class
Class I
17
Class IIa
Class IIb
Class III
Class II (US)
13
More classes (11)
Class A
Class B
Class C
Class D
IVD General
IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
Unclassified (FDA)
Not classified (FDA)
Verified
Validated only
Category (EMDN)
Browse by category
Apply filters
Reset
30 devices found
·
sorted by relevance
Key
Manufacturer: Dravon Medical Inc
×
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Peritoneal Dialysis Cycler Set (8UNIT)
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K812772
Active
Cleared 19 Oct 1981
Active
510(k)
510(k)
II
Cannula, Artery, Renal
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K780079
Active
Cleared 13 Feb 1978
Active
510(k)
510(k)
II
S3086 Arterial, S3087 Venous Neonatal Hemodialysis
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K873455
Active
Cleared 14 Sep 1987
Active
510(k)
510(k)
II
Hemostatic/Tube Occluding Forceps
Dravon Medical, Inc.
·
,
FDA registration: United States
Class I
FDA 510(k)
K800435
Active
Cleared 12 Mar 1980
Active
510(k)
510(k)
I
Stediflo Infusion Set
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K832739
Active
Cleared 22 Dec 1983
Active
510(k)
510(k)
II
Catheter, Beta-Cap-Peritoneal
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K782058
Active
Cleared 27 Feb 1979
Active
510(k)
510(k)
II
Terasaki Lymphocyte Transport Kit
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K760952
Active
Cleared 17 Jan 1977
Active
510(k)
510(k)
II
Forcep, Disp., A Clamp
Dravon Medical, Inc.
·
,
FDA registration: United States
Class I
FDA 510(k)
K771097
Active
Cleared 14 Jul 1977
Active
510(k)
510(k)
I
Decollating Tray
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K760995
Active
Cleared 6 Jan 1977
Active
510(k)
510(k)
II
Dap-Pak
Dravon Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K781755
Active
Cleared 15 Feb 1979
Active
510(k)
510(k)
II
Previous
Next
Showing 21-30 of 30