Atlas FDA

FTA-ABS TEST SYSTEM

FDA 510(k) clearance K781403 · decided 1978-08-21

Clearance details

K-number
K781403
Device name
FTA-ABS TEST SYSTEM
Applicant
Zeus Scientific, Inc.
Decision
Substantially Equivalent
Date received
1978-08-15
Decision date
1978-08-21
Days to decision
6 days
Clearance type
Traditional
Product code
GMS
Device class
2
Regulation number
866.3830
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
IMMUNO-PROD IND FLUORE TREPONE ANTIBODY ABSORPED (K853122)Immuno-Products Industries1985-09-19
FLUORESCENT TREPONEMEL ANTIBODY-ABSORB (K843613)Immuno-Products Industries1984-10-31

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ZEUS ELISA PARVOVIRUS B19 IGM TEST SYSTEM (P150042)Zeus Scientific, Inc.2017-09-19
ZEUS ELISA PARVOVIRUS B19 IGG TEST SYSTEM (P150045)Zeus Scientific, Inc.2017-09-19
FLUORO-CEP (R) PROGESTERONE (P900025/S001)Zeus Scientific, Inc.1992-04-21
FLUORO-CEP (R) PROGESTERONE (P900025/S002)Zeus Scientific, Inc.1992-04-17
FLUORO-CEP (R) PROGESTERONE (P900025)Zeus Scientific, Inc.1990-09-26