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)
47
FDA PMA
GUDID
Country / market
United States
47
Risk class
Class I
41
Class IIa
Class IIb
Class III
Class II (US)
6
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
47 devices found
·
sorted by relevance
Key
Manufacturer: Granite Diagnostics, Inc.
×
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Dipchex Dip-Slide Culture Sys
Granite Diagnostics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K830252
Active
Cleared 7 Mar 1983
Active
510(k)
510(k)
I
Thioglycollate Med. W/Vitamin K-1
Granite Diagnostics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K821864
Active
Cleared 13 Jul 1982
Active
510(k)
510(k)
I
Gramstain Set
Granite Diagnostics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K821977
Active
Cleared 22 Jul 1982
Active
510(k)
510(k)
I
Macate Broth
Granite Diagnostics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K823000
Active
Cleared 16 Nov 1982
Active
510(k)
510(k)
I
Columbia Agar With 5% Rabbit Blood
Granite Diagnostics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K780704
Active
Cleared 12 May 1978
Active
510(k)
510(k)
I
V Agar
Granite Diagnostics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K822702
Active
Cleared 30 Sep 1982
Active
510(k)
510(k)
I
Campy Thioglycollate (Tube)
Granite Diagnostics, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K812451
Active
Cleared 23 Sep 1981
Active
510(k)
510(k)
I
Previous
Next
Showing 41-47 of 47