Atlas FDA

COCCIDIOIDES ANTIGEN #CF10023X

FDA 510(k) clearance K791389 · decided 1979-08-16

Clearance details

K-number
K791389
Device name
COCCIDIOIDES ANTIGEN #CF10023X
Applicant
Immuno-Mycologics, Inc.
Decision
Substantially Equivalent
Date received
1979-07-11
Decision date
1979-08-16
Days to decision
36 days
Clearance type
Traditional
Product code
GMI
Device class
2
Regulation number
866.3135
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
OLYMPUS PK-TP SYSTEM REACTIVE CONTROL (K894617)Schiff & Co.1989-10-31
COCCIDIOIDES IMMUNODIFFUSION SYSTEM (K812190)American Scientific Products1981-08-31
FUNGAL IMMUNODIFFUSION SYSTEM (K812185)American Scientific Products1981-08-25
IMMUNODIFFUSION REAGENTS/SEROLOGICAL (K802129)Nolan Biological Laboratories, Inc.1980-09-26
CANDIDA ALBICANS, ANTIGEN (K792716)Meridian Diagnostics, Inc.1980-01-24
CANDIDA ALBICANS, ANTISERUM (K792713)Meridian Diagnostics, Inc.1980-01-23
COCCIDIOIDES IMMITIS, ANTIGEN (K792689)Meridian Diagnostics, Inc.1980-01-17
COCCIDIOIDES IMMITIS, ANTIGEN (K792682)Meridian Diagnostics, Inc.1980-01-17
CANDIDA IMMUNODIFFUSION KIT #CA1001 (K791383)Immuno-Mycologics, Inc.1979-08-16
CANDIDA IMMUNODIFFUSION KIT (K770527)I M, Inc.1978-03-17

Recalls involving this device

No recalls on record reference this clearance.