Atlas FDA

BRUCELLA IFA*

FDA 510(k) clearance K885112 · decided 1989-08-15

Clearance details

K-number
K885112
Device name
BRUCELLA IFA*
Applicant
Investigacion Farmaceutica S.A. DE C.V.
Decision
Substantially Equivalent
Date received
1988-12-12
Decision date
1989-08-15
Days to decision
246 days
Clearance type
Traditional
Product code
GSO
Device class
2
Regulation number
866.3085
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mexico, MX
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VISTA ANTIGEN BRUCELLA ABORTUS (K972394)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN BRUCELLA MELITENSIS (K972396)Lee Laboratories, Inc.1997-08-25
SAS BRUCELLA SUIS ANTIGEN (K952139)Sa Scientific, Inc.1995-07-18
SAS SALMONELLA H A ANTIGEN (K952137)Sa Scientific, Inc.1995-07-17
SAS FEBRILE ANTIGEN SET (K952131)Sa Scientific, Inc.1995-07-17
SAS BRUCELLA MELTIENSIS ANTIGEN (K952140)Sa Scientific, Inc.1995-07-17
SAS BRUCELLA ABORTUS ANTIGEN (K952147)Sa Scientific, Inc.1995-07-17
SAS SALMONELLA H B ANTIGEN (K952136)Sa Scientific, Inc.1995-07-17
SAS SALMONELLA H D ANTIGEN (K952135)Sa Scientific, Inc.1995-07-17
FEBRILE ANTIGEN KIT (K822663)Oxoid U.S.A., Inc.1982-09-21
AGGLUTINOTEST-BRUCELLA (K791449)Volu Sol Medical Industries1979-09-24

Recalls involving this device

No recalls on record reference this clearance.