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73 devices found
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Manufacturer: Azurmeds, Inc.
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Device · Manufacturer · Authorizations
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Class
Ltj 81004162343
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162131
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162336
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162654
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
GUDID
not on market
Withdrawn
GUDID
I
Ltj 81004162134
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162333
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162135
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162337
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162355
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
Ltj 81004162645
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
GUDID
not on market
Withdrawn
GUDID
I
Ltj 81004162340
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
GUDID
not on market
Withdrawn
GUDID
II
LTJ Screws and Washer
Azurmeds, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K200987
Active
Cleared 22 Sep 2020
Active
510(k)
510(k)
II
2 variants
LTJ Screws and Washer
K210268
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Showing 61-73 of 73