Atlas FDA

ASPERGILLUS SP, COMPLEMENT FIXATION

FDA 510(k) clearance K792700 · decided 1980-01-17

Clearance details

K-number
K792700
Device name
ASPERGILLUS SP, COMPLEMENT FIXATION
Applicant
Meridian Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1979-12-27
Decision date
1980-01-17
Days to decision
21 days
Clearance type
Traditional
Product code
JWT
Device class
1
Regulation number
866.3040
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

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

RecordFirmDate
REAGENTS FOR SERODIAGNOSIS OF ASPERGILL (K812740)Nolan Biological Laboratories, Inc.1981-10-20
ASPERGILLUS MYCELIAL ANTIGEN #CF10024X (K791387)Immuno-Mycologics, Inc.1979-08-16
ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVU (K790672)Diagnostica, Inc.1979-05-31
ASPERGILLUS MYCELIAL ANTIGEN (K760830)I M, Inc.1976-11-01

Recalls involving this device

No recalls on record reference this clearance.