Atlas FDA

TOXOGEN

FDA 510(k) clearance K981263 · decided 1998-08-06

Clearance details

K-number
K981263
Device name
TOXOGEN
Applicant
Instrumentation Laboratory CO
Decision
Substantially Equivalent
Date received
1998-04-07
Decision date
1998-08-06
Days to decision
121 days
Clearance type
Traditional
Product code
GMM
Device class
2
Regulation number
866.3780
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Bedford, MA, 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
ENZYME LINKED IMMUNOABSORBENT ASSAY, TOXOPLASMA GONDII (K952818)Pyramid Biological Corp.1995-11-20
HEM AVE-TOXO TITRATION HEMAGGLUTINATION TEST KIT (K851977)Si Sero-Immuno Diagnostics, Inc.1985-10-16
HEM AVE-TOXO SCREENING HEMAGGLUTINATION TEST KIT (K851976)Si Sero-Immuno Diagnostics, Inc.1985-10-16
POLYCHACO INDIRECT HEMAGGLUTINATION (K830870)Parasitic Disease Consultants1983-08-12
TOXOTEST-MT EIKEN KIT (K802452)Syn-Kit, Inc.1980-12-18
TXOCELL-IHA REAGENT SYSTEM (K790460)Calbiochem-Behring Corp.1979-05-25
TOXHA TEST (K771560)Burroughs Wellcome Co.1977-09-15

Recalls involving this device

No recalls on record reference this clearance.